Partially saturated tricyclic compounds and methods of making and using same

ABSTRACT

The invention provides tricyclic compounds and their use in treating medical disorders, such as obesity. Pharmaceutical compositions and methods of making various tricyclic compounds are provided. The compounds are contemplated to have activity against methionyl aminopeptidase 2.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No.14/116,023, filed Nov. 6, 2013, which is a national stage filing underU.S.C. §371 of PCT/US2012/036789, filed May 7, 2012, which claimspriority to U.S. Provisional Patent Application 61/559,856, filed Nov.15, 2011, and U.S. Provisional Patent Application 61/483,257, filed May6, 2011, all of which are incorporated by reference in their entirety.

BACKGROUND

Over 1.1 billion people worldwide are reported to be overweight. Obesityis estimated to affect over 90 million people in the United Statesalone. Twenty-five percent of the population in the United States overthe age of twenty is considered clinically obese. While being overweightor obese presents problems (for example restriction of mobility,discomfort in tight spaces such as theater or airplane seats, socialdifficulties, etc.), these conditions, in particular clinical obesity,affect other aspects of health, i.e., diseases and other adverse healthconditions associated with, exacerbated by, or precipitated by beingoverweight or obese. The estimated mortality from obesity-relatedconditions in the United States is over 300,000 annually (O'Brien et al.Amer J Surgery (2002) 184:4S-8S; and Hill et al. (1998) Science,280:1371).

There is no curative treatment for being overweight or obese.Traditional pharmacotherapies for treating an overweight or obesesubject, such as serotonin and noradrenergic re-uptake inhibitors,noradrenergic re-uptake inhibitors, selective serotonin re-uptakeinhibitors, intestinal lipase inhibitors, or surgeries such as stomachstapling or gastric banding, have been shown to provide minimalshort-term benefits or significant rates of relapse, and have furthershown harmful side-effects to patients.

MetAP2 encodes a protein that functions at least in part byenzymatically removing the amino terminal methionine residue fromcertain newly translated proteins such as glyceraldehyde-3-phosphatedehydrogenase (Warder et al. (2008) J Proteome Res 7:4807). Increasedexpression of the MetAP2 gene has been historically associated withvarious forms of cancer. Molecules inhibiting the enzymatic activity ofMetAP2 have been identified and have been explored for their utility inthe treatment of various tumor types (Wang et al. (2003) Cancer Res.63:7861) and infectious diseases such as microsporidiosis,leishmaniasis, and malaria (Zhang et al. (2002) J. Biomed. Sci. 9:34).Notably, inhibition of MetAP2 activity in obese and obese-diabeticanimals leads to a reduction in body weight in part by increasing theoxidation of fat and in part by reducing the consumption of food(Rupnick et al. (2002) Proc. Natl. Acad. Sci. USA 99:10730).

Such MetAP2 inhibitors may be useful as well for patients with excessadiposity and conditions related to adiposity including type 2 diabetes,hepatic steatosis, and cardiovascular disease (via e.g. amelioratinginsulin resistance, reducing hepatic lipid content, and reducing cardiacworkload). Accordingly, compounds capable of modulating MetAP2 areneeded to address the treatment of obesity and related diseases as wellas other ailments favorably responsive to MetAP2 modulator treatment.

SUMMARY

The invention provides, for example, compounds which may be modulatorsof MetAP2, and their use as medicinal agents, processes for theirpreparation, and pharmaceutical compositions containing them as anactive ingredient both alone or in combination with other agents, aswell as provides for their use as medicaments and/or in the manufactureof medicaments for the inhibition of MetAP2 activity in warm-bloodedanimals such as humans. In particular this invention relates tocompounds useful for the treatment of obesity, type 2 diabetes, andother obesity-associated conditions. Also provided are pharmaceuticalcompositions comprising at least one disclosed compound and apharmaceutically acceptable carrier.

In an embodiment, provided herein are compounds represented by formula Iand II:

or

or pharmaceutically acceptable salts, stereoisomers, esters or prodrugsthereof, where A, B¹, B², D¹, D², R^(A1), R^(A2), R^(B1), R^(B2), Y, X¹,X², and n are as defined herein.

DETAILED DESCRIPTION

The features and other details of the disclosure will now be moreparticularly described. Before further description of the presentinvention, certain terms employed in the specification, examples andappended claims are collected here. These definitions should be read inlight of the remainder of the disclosure and as understood by a personof skill in the art. Unless defined otherwise, all technical andscientific terms used herein have the same meaning as commonlyunderstood by a person of ordinary skill in the art.

Definitions

“Treating” includes any effect, e.g., lessening, reducing, modulating,or eliminating, that results in the improvement of the condition,disease, disorder and the like.

The term “alkenyl” as used herein refers to an unsaturated straight orbranched hydrocarbon having at least one carbon-carbon double bond.Exemplary alkenyl groups include, but are not limited to, a straight orbranched group of 2-6 or 3-4 carbon atoms, referred to herein asC₂₋₆alkenyl, and C₃₋₄alkenyl, respectively. Exemplary alkenyl groupsinclude, but are not limited to, vinyl, allyl, butenyl, pentenyl, etc.

The term “alkoxy” as used herein refers to a straight or branched alkylgroup attached to oxygen (alkyl-O—). Exemplary alkoxy groups include,but are not limited to, alkoxy groups of 1-6 or 2-6 carbon atoms,referred to herein as C₁₋₆alkoxy, and C₂₋₆alkoxy, respectively.Exemplary alkoxy groups include, but are not limited to methoxy, ethoxy,isopropoxy, etc.

The term “alkoxyalkyl” as used herein refers to a straight or branchedalkyl group attached to oxygen, attached to a second straight orbranched alkyl group (alkyl-O-alkyl-). Exemplary alkoxyalkyl groupsinclude, but are not limited to, alkoxyalkyl groups in which each of thealkyl groups independently contains 1-6 carbon atoms, referred to hereinas C₁₋₆alkoxy-C₁₋₆alkyl. Exemplary alkoxyalkyl groups include, but arenot limited to methoxymethyl, 2-methoxyethyl, 1-methoxyethyl,2-methoxypropyl, ethoxymethyl, 2-isopropoxyethyl etc.

The term “alkyoxycarbonyl” as used herein refers to a straight orbranched alkyl group attached to oxygen, attached to a carbonyl group(alkyl-O—C(O)—). Exemplary alkoxycarbonyl groups include, but are notlimited to, alkoxycarbonyl groups of 1-6 carbon atoms, referred toherein as C₁₋₆alkoxycarbonyl. Exemplary alkoxycarbonyl groups include,but are not limited to, methoxycarbonyl, ethoxycarbonyl,t-butoxycarbonyl, etc.

The term “alkenyloxy” used herein refers to a straight or branchedalkenyl group attached to oxygen (alkenyl-O—). Exemplary alkenyloxygroups include, but are not limited to, groups with an alkenyl group of3-6 carbon atoms, referred to herein as C₃₋₆alkenyloxy. Exemplary“alkenyloxy” groups include, but are not limited to allyloxy,butenyloxy, etc.

The term “alkynyloxy” used herein refers to a straight or branchedalkynyl group attached to oxygen (alkynyl-O). Exemplary alkynyloxygroups include, but are not limited to, groups with an alkynyl group of3-6 carbon atoms, referred to herein as C₃₋₆alkynyloxy. Exemplaryalkynyloxy groups include, but are not limited to, propynyloxy,butynyloxy, etc.

The term “alkyl” as used herein refers to a saturated straight orbranched hydrocarbon. Exemplary alkyl groups include, but are notlimited to, straight or branched hydrocarbons of 1-6, 1-4, or 1-3 carbonatoms, referred to herein as C₁₋₆alkyl, C₁₋₄alkyl, and C₁₋₃alkyl,respectively. Exemplary alkyl groups include, but are not limited to,methyl, ethyl, propyl, isopropyl, 2-methyl-1-butyl, 3-methyl-2-butyl,2-methyl-1-pentyl, 3-methyl-1-pentyl, 4-methyl-1-pentyl,2-methyl-2-pentyl, 3-methyl-2-pentyl, 4-methyl-2-pentyl,2,2-dimethyl-1-butyl, 3,3-dimethyl-1-butyl, 2-ethyl-1-butyl, butyl,isobutyl, t-butyl, pentyl, isopentyl, neopentyl, hexyl, etc.

The term “alkylcarbonyl” as used herein refers to a straight or branchedalkyl group attached to a carbonyl group (alkyl-C(O)—). Exemplaryalkylcarbonyl groups include, but are not limited to, alkylcarbonylgroups of 1-6 atoms, referred to herein as C₁₋₆alkylcarbonyl groups.Exemplary alkylcarbonyl groups include, but are not limited to, acetyl,propanoyl, isopropanoyl, butanoyl, etc.

The term “alkynyl” as used herein refers to an unsaturated straight orbranched hydrocarbon having at least one carbon-carbon triple bond.Exemplary alkynyl groups include, but are not limited to, straight orbranched groups of 2-6, or 3-6 carbon atoms, referred to herein asC₂₋₆alkynyl, and C₃₋₆alkynyl, respectively. Exemplary alkynyl groupsinclude, but are not limited to, ethynyl, propynyl, butynyl, pentynyl,hexynyl, methylpropynyl, etc.

The term “carbonyl” as used herein refers to the radical —C(O)—.

The term “cyano” as used herein refers to the radical —CN.

The term “cycloalkoxy” as used herein refers to a cycloalkyl groupattached to oxygen (cycloalkyl-O—). Exemplary cycloalkoxy groupsinclude, but are not limited to, cycloalkoxy groups of 3-6 carbon atoms,referred to herein as C₃₋₆cycloalkoxy groups. Exemplary cycloalkoxygroups include, but are not limited to, cyclopropoxy, cyclobutoxy,cyclohexyloxy, etc

The terms “cycloalkyl” or a “carbocyclic group” as used herein refers toa saturated or partially unsaturated hydrocarbon group of, for example,3-6, or 4-6 carbons, referred to herein as C₃₋₆cycloalkyl orC₄₋₆cycloalkyl, respectively. Exemplary cycloalkyl groups include, butare not limited to, cyclohexyl, cyclopentyl, cyclopentenyl, cyclobutylor cyclopropyl.

The terms “halo” or “halogen” as used herein refer to F, Cl, Br, or I.

The terms “heteroaryl” or “heteroaromatic group” as used herein refersto a monocyclic aromatic 5-6 membered ring system containing one or moreheteroatoms, for example one to three heteroatoms, such as nitrogen,oxygen, and sulfur. Where possible, said heteroaryl ring may be linkedto the adjacent radical though carbon or nitrogen. Examples ofheteroaryl rings include but are not limited to furan, thiophene,pyrrole, thiazole, oxazole, isothiazole, isoxazole, imidazole, pyrazole,triazole, pyridine or pyrimidine etc.

The terms “heterocyclyl” or “heterocyclic group” are art-recognized andrefer to saturated or partially unsaturated, 4-10 membered ringstructures, including bridged or fused rings, and whose ring structuresinclude one to three heteroatoms, such as nitrogen, oxygen, and sulfur.Where possible, heterocyclyl rings may be linked to the adjacent radicalthrough carbon or nitrogen. Examples of heterocyclyl groups include, butare not limited to, pyrrolidine, piperidine, morpholine, thiomorpholine,piperazine, oxetane, azetidine, tetrahydrofuran or dihydrofuran etc.

The term “heterocyclyloxy” as used herein refers to a heterocyclyl groupattached to oxygen (heterocyclyl-O—).

The term “heteroaryloxy” as used herein refers to a heteroaryl groupattached to oxygen (heteroaryl-O—).

The terms “hydroxy” and “hydroxyl” as used herein refers to the radical—OH.

The term “oxo” as used herein refers to the radical ═O.

“Pharmaceutically or pharmacologically acceptable” include molecularentities and compositions that do not produce an adverse, allergic orother untoward reaction when administered to an animal, or a human, asappropriate. For human administration, preparations should meetsterility, pyrogenicity, and general safety and purity standards asrequired by FDA Office of Biologics standards.

The term “pharmaceutically acceptable carrier” or “pharmaceuticallyacceptable excipient” as used herein refers to any and all solvents,dispersion media, coatings, isotonic and absorption delaying agents, andthe like, that are compatible with pharmaceutical administration. Theuse of such media and agents for pharmaceutically active substances iswell known in the art. The compositions may also contain other activecompounds providing supplemental, additional, or enhanced therapeuticfunctions.

The term “pharmaceutical composition” as used herein refers to acomposition comprising at least one compound as disclosed hereinformulated together with one or more pharmaceutically acceptablecarriers.

“Individual,” “patient,” or “subject” are used interchangeably andinclude any animal, including mammals, preferably mice, rats, otherrodents, rabbits, dogs, cats, swine, cattle, sheep, horses, or primates,and most preferably humans. The compounds of the invention can beadministered to a mammal, such as a human, but can also be administeredto other mammals such as an animal in need of veterinary treatment,e.g., domestic animals (e.g., dogs, cats, and the like), farm animals(e.g., cows, sheep, pigs, horses, and the like) and laboratory animals(e.g., rats, mice, guinea pigs, and the like). The mammal treated in themethods of the invention is desirably a mammal in which treatment ofobesity or weight loss is desired. “Modulation” includes antagonism(e.g., inhibition), agonism, partial antagonism and/or partial agonism.

In the present specification, the term “therapeutically effectiveamount” means the amount of the subject compound that will elicit thebiological or medical response of a tissue, system or animal, (e.g.mammal or human) that is being sought by the researcher, veterinarian,medical doctor or other clinician. The compounds of the invention areadministered in therapeutically effective amounts to treat a disease.Alternatively, a therapeutically effective amount of a compound is thequantity required to achieve a desired therapeutic and/or prophylacticeffect, such as an amount which results in weight loss.

The term “pharmaceutically acceptable salt(s)” as used herein refers tosalts of acidic or basic groups that may be present in compounds used inthe compositions. Compounds included in the present compositions thatare basic in nature are capable of forming a wide variety of salts withvarious inorganic and organic acids. The acids that may be used toprepare pharmaceutically acceptable acid addition salts of such basiccompounds are those that form non-toxic acid addition salts, i.e., saltscontaining pharmacologically acceptable anions, including, but notlimited to, malate, oxalate, chloride, bromide, iodide, nitrate,sulfate, bisulfate, phosphate, acid phosphate, isonicotinate, acetate,lactate, salicylate, citrate, tartrate, oleate, tannate, pantothenate,bitartrate, ascorbate, succinate, maleate, gentisinate, fumarate,gluconate, glucaronate, saccharate, formate, benzoate, glutamate,methanesulfonate, ethanesulfonate, benzenesulfonate, p-toluenesulfonateand pamoate (i.e., 1,1′-methylene-bis-(2-hydroxy-3-naphthoate)) salts.Compounds included in the present compositions that are acidic in natureare capable of forming base salts with various pharmacologicallyacceptable cations. Examples of such salts include alkali metal oralkaline earth metal salts, particularly calcium, magnesium, sodium,lithium, zinc, potassium, and iron salts. Compounds included in thepresent compositions that include a basic or acidic moiety may also formpharmaceutically acceptable salts with various amino acids. Thecompounds of the disclosure may contain both acidic and basic groups;for example, one amino and one carboxylic acid group. In such a case,the compound can exist as an acid addition salt, a zwitterion, or a basesalt.

The compounds of the disclosure may contain one or more chiral centersand, therefore, exist as stereoisomers. The term “stereoisomers” whenused herein consist of all enantiomers or diastereomers. These compoundsmay be designated by the symbols “(+),” “(−),” “R” or “S,” depending onthe configuration of substituents around the stereogenic carbon atom,but the skilled artisan will recognize that a structure may denote achiral center implicitly. The present invention encompasses variousstereoisomers of these compounds and mixtures thereof. Mixtures ofenantiomers or diastereomers may be designated “(±)” in nomenclature,but the skilled artisan will recognize that a structure may denote achiral center implicitly.

The compounds of the disclosure may contain one or more double bondsand, therefore, exist as geometric isomers resulting from thearrangement of substituents around a carbon-carbon double bond. Thesymbol

denotes a bond that may be a single, double or triple bond as describedherein. Substituents around a carbon-carbon double bond are designatedas being in the “Z” or “E” configuration wherein the terms “Z” and “E”are used in accordance with IUPAC standards. Unless otherwise specified,structures depicting double bonds encompass both the “E” and “Z”isomers. Substituents around a carbon-carbon double bond alternativelycan be referred to as “cis” or “trans,” where “cis” representssubstituents on the same side of the double bond and “trans” representssubstituents on opposite sides of the double bond.

Compounds of the disclosure may contain a carbocyclic or heterocyclicring and therefore, exist as geometric isomers resulting from thearrangement of substituents around the ring. The arrangement ofsubstituents around a carbocyclic or heterocyclic ring are designated asbeing in the “Z” or “E” configuration wherein the terms “Z” and “E” areused in accordance with IUPAC standards. Unless otherwise specified,structures depicting carbocyclic or heterocyclic rings encompass both“Z” and “E” isomers. Substituents around a carbocyclic or heterocyclicrings may also be referred to as “cis” or “trans”, where the term “cis”represents substituents on the same side of the plane of the ring andthe term “trans” represents substituents on opposite sides of the planeof the ring. Mixtures of compounds wherein the substituents are disposedon both the same and opposite sides of plane of the ring are designated“cis/trans.”

Individual enantiomers and diasteriomers of compounds of the presentinvention can be prepared synthetically from commercially availablestarting materials that contain asymmetric or stereogenic centers, or bypreparation of racemic mixtures followed by resolution methods wellknown to those of ordinary skill in the art. These methods of resolutionare exemplified by (1) attachment of a mixture of enantiomers to achiral auxiliary, separation of the resulting mixture of diastereomersby recrystallization or chromatography and liberation of the opticallypure product from the auxiliary, (2) salt formation employing anoptically active resolving agent, (3) direct separation of the mixtureof optical enantiomers on chiral liquid chromatographic columns or (4)kinetic resolution using stereoselective chemical or enzymatic reagents.Racemic mixtures can also be resolved into their component enantiomersby well known methods, such as chiral-phase liquid chromatography orcrystallizing the compound in a chiral solvent. Stereoselectivesyntheses, a chemical or enzymatic reaction in which a single reactantforms an unequal mixture of stereoisomers during the creation of a newstereocenter or during the transformation of a pre-existing one, arewell known in the art. Stereoselective syntheses encompass both enantio-and diastereoselective transformations, and may involve the use ofchiral auxiliaries. For examples, see Carreira and Kvaerno, Classics inStereoselective Synthesis, Wiley-VCH: Weinheim, 2009.

The compounds disclosed herein can exist in solvated as well asunsolvated forms with pharmaceutically acceptable solvents such aswater, ethanol, and the like, and it is intended that the inventionembrace both solvated and unsolvated forms. In one embodiment, thecompound is amorphous. In one embodiment, the compound is a singlepolymorph. In another embodiment, the compound is a mixture ofpolymorphs. In another embodiment, the compound is in a crystallineform.

The invention also embraces isotopically labeled compounds of theinvention which are identical to those recited herein, except that oneor more atoms are replaced by an atom having an atomic mass or massnumber different from the atomic mass or mass number usually found innature. Examples of isotopes that can be incorporated into compounds ofthe invention include isotopes of hydrogen, carbon, nitrogen, oxygen,phosphorus, sulfur, fluorine and chlorine, such as ²H, ³H, ¹³C, ¹⁴C,¹⁵N, ¹⁸O, ¹⁷O, ³¹P, ³²P, ³⁵S, ¹⁸F, and ³⁶Cl, respectively. For example,a compound of the invention may have one or more H atom replaced withdeuterium.

Certain isotopically-labeled disclosed compounds (e.g., those labeledwith ³H and ¹⁴C) are useful in compound and/or substrate tissuedistribution assays. Tritiated (i.e., ³H) and carbon-14 (i.e., ¹⁴C)isotopes are particularly preferred for their ease of preparation anddetectability. Further, substitution with heavier isotopes such asdeuterium (i.e., ²H) may afford certain therapeutic advantages resultingfrom greater metabolic stability (e.g., increased in vivo half-life orreduced dosage requirements) and hence may be preferred in somecircumstances. Isotopically labeled compounds of the invention cangenerally be prepared by following procedures analogous to thosedisclosed in the examples herein by substituting an isotopically labeledreagent for a non-isotopically labeled reagent.

The term “prodrug” refers to compounds that are transformed in vivo toyield a disclosed compound or a pharmaceutically acceptable salt,hydrate or solvate of the compound. The transformation may occur byvarious mechanisms (such as by esterase, amidase, phosphatase, oxidativeand or reductive metabolism) in various locations (such as in theintestinal lumen or upon transit of the intestine, blood or liver).Prodrugs are well known in the art (for example, see Rautio,Kumpulainen, et al, Nature Reviews Drug Discovery 2008, 7, 255). Forexample, if a compound of the invention or a pharmaceutically acceptablesalt, hydrate or solvate of the compound contains a carboxylic acidfunctional group, a prodrug can comprise an ester formed by thereplacement of the hydrogen atom of the acid group with a group such as(C₁₋₈)alkyl, (C₂₋₁₂)alkylcarbonyloxymethyl, 1-(alkylcarbonyloxy)ethylhaving from 4 to 9 carbon atoms, 1-methyl-1-(alkylcarbonyloxy)-ethylhaving from 5 to 10 carbon atoms, alkoxycarbonyloxymethyl having from 3to 6 carbon atoms, 1-(alkoxycarbonyloxy)ethyl having from 4 to 7 carbonatoms, 1-methyl-1-(alkoxycarbonyloxy)ethyl having from 5 to 8 carbonatoms, N-(alkoxycarbonyl)aminomethyl having from 3 to 9 carbon atoms,1-(N-(alkoxycarbonyl)amino)ethyl having from 4 to 10 carbon atoms,3-phthalidyl, 4-crotonolactonyl, gamma-butyrolacton-4-yl,di-N,N—(C₁₋₂)alkylamino(C₂₋₃)alkyl (such as (3-dimethylaminoethyl),carbamoyl-(C₁₋₂)alkyl, N,N-di(C₁₋₂)alkylcarbamoyl-(C₁₋₂)alkyl andpiperidino-, pyrrolidino- or morpholino(C₂₋₃)alkyl.

Similarly, if a compound of the invention contains an alcohol functionalgroup, a prodrug can be formed by the replacement of the hydrogen atomof the alcohol group with a group such as (C₁₋₆)alkylcarbonyloxymethyl,1-((C₁₋₆)alkylcarbonyloxy)ethyl,1-methyl-1-((C₁₋₆)alkylcarbonyloxy)ethyl (C₁₋₆)alkoxycarbonyloxymethyl,N—(C₁₋₆)alkoxycarbonylaminomethyl, succinoyl, (C₁₋₆)alkylcarbonyl,α-amino(C₁₋₄)alkylcarbonyl, arylalkylcarbonyl and α-aminoalkylcarbonyl,or α-aminoalkylcarbonyl-α-aminoalkylcarbonyl, where eacht-aminoalkylcarbonyl group is independently selected from the naturallyoccurring L-amino acids, P(O)(OH)₂, —P(O)(O(C₁₋₆)alkyl)₂ or glycosyl(the radical resulting from the removal of a hydroxyl group of thehemiacetal form of a carbohydrate).

If a compound of the invention incorporates an amine functional group, aprodrug can be formed, for example, by creation of an amide orcarbamate, an N-alkylcarbonyloxyalkyl derivative, an(oxodioxolenyl)methyl derivative, an N-Mannich base, imine or enamine.In addition, a secondary amine can be metabolically cleaved to generatea bioactive primary amine, or a tertiary amine can metabolically cleavedto generate a bioactive primary or secondary amine. For examples, seeSimplicio, et al., Molecules 2008, 13, 519 and references therein.

I. Tricyclic Compounds

In certain embodiments, the present invention provides compounds ofFormula I or Formula II:

or

wherein

B¹ may be a 3-6 membered saturated or partially unsaturated heterocyclicor carbocyclic ring;

B² may be a 3-6 membered saturated heterocyclic or carbocyclic ring;

wherein the ring B¹ or B² may optionally be substituted by one or morefluorine atoms on any of the available carbon atoms

D¹ may be a 5-7 membered heterocyclic, carbocyclic, heteroaromatic oraromatic ring;

D² may be a 5-7 membered heterocyclic or carbocyclic ring;

wherein B¹ is fused to D¹ such that the two atoms shared by B¹ and D¹are both carbon and B² is fused to D² such that the two atoms shared byB² and D² are both carbon; and wherein for Formula I the bond common toboth the B¹ and D¹ rings may be a single or double bond;

X¹ may be selected from the group consisting of: ⁺—C(R^(D1)R^(D2))—*,⁺—W¹—*, ⁺—C(R^(D1)R^(D2))—C(R^(D5)R^(D6))—*, ⁺—C(R^(C1))═C(R^(C2))—*,⁺—W²—C(R^(D5)R^(D6))—*, ⁺—W²—C(O)—*, ⁺—C(R^(D1)R^(D2))—W⁴—*,⁺—N═C(R^(C2))—*, ⁺—C(R^(C1))═N—*,⁺—C(R^(D1)R^(D2))—C(R^(D3)R^(D4))—C(R^(D5)R^(D6))—*,⁺—W²—C(R^(D3)R^(D4))—C(R^(D5)R^(D6))—*, ⁺—W²—C(O)—C(R^(D5)R^(D6))—*,⁺—C(R^(D1)R^(D2))—W³—C(R^(D5)R^(D6))—*, ⁺—C(R^(D1)R^(D2))—W³—C(O)—*,⁺—C(R^(D1)R^(D2))—C(R^(D3)R^(D4))—W⁴—* and ⁺—C(R^(D1)R^(D2))—C(O)—W⁴—*;wherein the ⁺ and * indicate the attachment points of X¹ as indicated inFormula I;

X² may be selected from the group consisting of: ⁺—C(R^(D1)R^(D2))—*,⁺—W¹—*, ⁺—C(R^(D1)R^(D2))—C(R^(D5)R^(D6))—*, ⁺—W²—C(R^(D5)R^(D6))—*,⁺—W²—C(O)—*, ⁺—C(R^(D1)R^(D2))—W⁴—*,⁺—C(R^(D1)R^(D2))—C(R^(D3)R^(D4))—C(R^(D5)R^(D6))—*,⁺—W²—C(R^(D3)R^(D4))—C(R^(D5)R^(D6))*, ⁺—W²—C(O)—C(R^(D5)R^(D6))—*,⁺—C(R^(D1)R^(D2))_W³—C(R^(D5)R^(D6))—*, ⁺—C(R^(D1)R^(D2))—W³—C(O)—*,⁺—C(R^(D1)R^(D2))—C(R^(D3)R^(D4))—W⁴—* and ⁺—C(R^(D1)R^(D2))—C(O)—W⁴—*;wherein the ⁺ and * indicate the attachment points of X² as indicated inFormula II;

Y may be selected from the group consisting of: a bond, *—CH₂—^(#),*—O—^(#), *—CH₂—CH₂—^(#), *—O—CH₂—^(#), *—CH₂—O—^(#),*—CH₂—CH₂—CH₂—^(#), *—O—CH₂—CH₂—^(#) and *—CH₂—O—CH₂—^(#); wherein the *and ^(#) indicate the attachment points of Y as indicated in Formula Ior Formula II;

W¹ may be selected from the group consisting of O, S, or N(R^(N1));

W² may be selected from the group consisting of O or N(R^(N2));

W³ may be selected from the group consisting of O or N(R^(N3));

W⁴ may be selected from the group consisting of O or N(R^(N4));

A may be a ring selected from the group consisting of phenyl, a 5-6membered heteroaryl having 1, 2 or 3 heteroatoms each selected from S, Nor O, and a 4-7 membered heterocycle having 1, 2 or 3 heteroatoms eachselected from N or O;

R^(B1) and R^(B2) are independently selected from the group consistingof H, F, OH, CN, C₁₋₂alkoxy or C₁₋₃alkyl; wherein C₁₋₃alkyl andC₁₋₂alkoxy are optionally substituted by a group selected from OH,C₁₋₂alkoxy, CN or one or more fluorine atoms;

R^(A1) may be selected, independently for each occurrence, from thegroup consisting of hydrogen, hydroxyl, cyano, halogen, C₁₋₄alkyl orC₁₋₃alkoxy; wherein C₁₋₄alkyl, or C₁₋₃alkoxy may be optionallysubstituted by one or more fluorines;

n may be 1 or 2;

R^(A2) may be selected from the group consisting of hydrogen,R^(i)R^(j)N—, heterocyclyl, heterocyclyloxy and heterocyclyl-(NR^(a))—;wherein said heterocyclyl may optionally be substituted by one or moresubstituents selected from R^(g) and wherein if said heterocyclylcontains a —NH moiety that nitrogen may optionally be substituted by oneor more groups R^(h); or

R^(A2) may be selected from the group consisting of: C₁₋₆alkyl,C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy, C₃₋₆alkenyloxy,C₃₋₆alkynyloxy, C₃₋₆cycloalkoxy, C₁₋₆alkyl-S(O)_(w)— (wherein w is 0, 1or 2), C₁₋₆alkyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))-carbonyl-,C₁₋₆alkylcarbonyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))-carbonyl-N(R^(a))—,C₁₋₆alkyl-N(R^(a))—SO₂—, C₁₋₆alkyl-SO₂—N(R^(a))—,C₁₋₆alkoxycarbonyl-N(R^(a))—, C₁₋₆alkylcarbonyl-N(R^(a))—C₁₋₆alkyl-,C₁₋₆alkyl-N(R^(a))-carbonyl-C₁₋₆alkyl-, C₁₋₆alkoxyC₁₋₆alkyl-; whereinC₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy,C₃₋₆alkenyloxy, C₃₋₆alkynyloxy, C₃₋₆cycloalkoxy, C₁₋₆alkyl-S(O)_(w)—,C₁₋₆alkyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))-carbonyl-,C₁₋₆alkylcarbonyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))-carbonyl-N(R^(a))—,C₁₋₆alkyl-N(R^(a))—SO₂—, C₁₋₆alkyl-SO₂—N(R^(a)),C₁₋₆alkoxycarbonyl(R^(a))—, C₁₋₆alkylcarbonyl-N(R^(a))C₁₋₆alkyl-,C₁₋₆alkyl-N(R^(a))-carbonyl-C₁₋₆alkyl-, C₁₋₆alkoxy-C₁₋₆alkyl mayoptionally be substituted by R^(P), phenyl, phenoxy, heteroaryl,heteroaryloxy, heteroaryl-(NR^(a))—, heterocyclyl, heterocyclyloxy orheterocyclyl-N(R^(a))—; and wherein said heteroaryl or phenyl mayoptionally be substituted with one or more substituents selected fromR^(f); and wherein said heterocyclyl may optionally be substituted byone or more substituents selected from R^(g); and wherein if saidheterocyclyl contains a —NH moiety that nitrogen may optionally besubstituted by one or more groups R^(h);

R^(D1) and R^(D2) may be each independently selected from the groupconsisting of hydrogen, fluorine, hydroxyl, C₁₋₂alkyl or C₁₋₂alkoxy;wherein the C₁₋₂alkyl and C₁₋₂alkoxy may optionally be substituted byone or more fluorine atoms or a group selected from cyano or hydroxyl;

R^(D3) and R^(D4) may be each independently selected from the groupconsisting of hydrogen, fluorine, hydroxyl, cyano, C₁₋₃alkyl orC₁₋₃alkoxy; wherein the C₁₋₃ alkyl and C₁₋₃ alkoxy may optionally besubstituted by one or more fluorine atoms or a group selected fromcyano, hydroxyl or N(R^(a)R^(b));

R^(D5) and R^(D6) may be each independently selected from the groupconsisting of hydrogen, fluorine, hydroxyl, cyano, C₁₋₂alkyl orC₁₋₂alkoxy; wherein the C₁₋₂alkyl and C₁₋₂alkoxy may optionally besubstituted by one or more fluorine atoms or a group selected fromcyano, hydroxyl or N(R^(a)R^(b));

R^(C1) may be selected from the group consisting of hydrogen, halogen,C₁₋₂alkyl or C₁₋₂alkoxy; wherein the C₁₋₂alkyl or C₁₋₂alkoxy mayoptionally be substituted by one or more fluorine atoms;

R^(C2) may be selected from the group consisting of hydrogen, halogen,hydroxyl, cyano, C₁₋₂alkyl or C₁₋₂alkoxy; wherein the C₁₋₂alkyl andC₁₋₂alkoxy may optionally be substituted by one or more fluorine atomsor a group selected from cyano, hydroxyl or N(R^(a)R^(b));

R^(N1) may be selected from the group consisting of hydrogen orC₁₋₂alkyl;

R^(N2) may be selected from the group consisting of hydrogen orC₁₋₂alkyl;

R^(N3) may be selected from the group consisting of hydrogen, C₁₋₃alkylor C₁₋₂alkylcarbonyl; wherein the C₁₋₃alkyl and C₁₋₂alkylcarbonyl mayoptionally be substituted by one or more fluorine atoms or a groupselected from cyano, hydroxyl or N(R^(a)R^(b));

R^(N4) may be selected from the group consisting of hydrogen, C₁₋₃alkylor C₁₋₂alkylcarbonyl; wherein the C₁₋₃alkyl and C₁₋₂alkylcarbonyl mayoptionally be substituted by one or more fluorine atoms or a groupselected from cyano, hydroxyl or N(R^(a)R^(b));

R^(a) and R^(b) may be independently selected, for each occurrence, fromthe group consisting of hydrogen and C₁₋₃alkyl; wherein C₁₋₃alkyl mayoptionally be substituted by one or more substituents selected fromfluorine, cyano, oxo and hydroxyl;

or R^(a) and R^(b), together with the nitrogen to which they areattached, may form a 4-6 membered heterocyclic ring, which may have anadditional heteroatom selected from O, S, or N; wherein the 4-6 memberedheterocyclic ring may optionally be substituted by one or moresubstituents selected from the group consisting of fluorine, cyano, oxoor hydroxyl;

R^(f) may be independently selected, for each occurrence, from the groupconsisting of R^(P), hydrogen, C₁₋₆alkyl, C₃₋₆cycloalkyl, C₂₋₆alkenyl,C₂₋₆alkynyl, C₁₋₆alkoxy, C₁₋₆alkyl-S(O)_(w)—, (wherein w is 0, 1 or 2),C₁₋₆alkylcarbonyl-N(R^(a))— and C₁₋₆alkoxycarbonyl-N(R^(a))—; whereinC₁₋₆alkyl, C₃₋₆cycloalkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₁₋₆alkoxy,C₁₋₆alkyl-S(O)_(w)—, C₁₋₆alkylcarbonyl-N(R^(a))—,C₁₋₆alkoxycarbonyl-N(R^(a))— may be optionally substituted by one ormore substituents selected from R^(P);

R^(g) may be independently selected for each occurrence from the groupconsisting of R^(P), hydrogen, oxo, C₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl,C₃₋₆cycloalkyl, C₁₋₆alkoxy, C₁₋₆alkyl-S(O)_(w)—, (wherein w is 0, 1 or2), C₁₋₆alkylcarbonyl-N(R^(a))— and C₁₋₆alkoxycarbonyl-N(R^(a))—;wherein C₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy,C₁₋₆alkyl-S(O)_(w)—, C₁₋₆alkylcarbonyl-N(R^(a))—,C₁₋₆alkoxycarbonyl-N(R^(a))— may be optionally substituted by one ormore substituents selected from R^(P);

R^(h) may be independently selected for each occurrence from the groupconsisting of hydrogen, C₁₋₆alkyl, C₃₋₆alkenyl, C₃₋₆alkynyl,C₃₋₆cycloalkyl, C₁₋₆alkyl-S(O)₂—, C₁₋₆alkoxycarbonyl-,R^(i)R^(j)N-carbonyl- and R^(i)R^(j)N—SO₂—; wherein C₁₋₆alkyl,C₃₋₆alkenyl, C₃₋₆alkynyl C₃₋₆cycloalkyl and C₁₋₆alkyl-S(O)₂—,C₁₋₆alkylcarbonyl- may optionally be substituted by one or moresubstituents selected from R^(P);

R^(i) and R^(j) may be selected independently for each occurrence fromthe group consisting of hydrogen, C₁₋₄alkyl C₃₋₆cycloalkyl, heterocyclyland heterocyclylcarbonyl; wherein C₁₋₄alkyl and C₃₋₆cycloalkyl may beoptionally substituted by one or more substituents selected fromfluorine, hydroxyl, cyano, R^(a)R^(b)N—, R^(a)R^(b)N-carbonyl- andC₁₋₃alkoxy and wherein heterocyclyl and heterocyclylcarbonyl may beoptionally substituted by one or more substituents selected fromC₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy,halo-C₁₋₆-alkyl, hydroxyl-C₁₋₆-alkyl, R^(a)R^(b)N—C₁₋₆alkyl- andC₁₋₆-alkoxy-C₁₋₆-alkyl group; and wherein if said heterocyclyl orheterocyclylcarbonyl contains a —NH moiety that nitrogen may optionallybe substituted by one or more groups C₁₋₆alkyl, C₃₋₆alkenyl,C₃₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkyl-S(O)₂— and C₁₋₆-alkylcarbonyl;

-   -   or R^(i) and R^(j) taken together with the nitrogen to which        they are attached may form a 4-7 membered heterocyclic ring,        which may have an additional heteroatom selected from O, S, or        N; wherein the 4-7 membered heterocyclic ring may be optionally        substituted on carbon by one or more substituents selected from        the group consisting of fluorine, hydroxyl, oxo, cyano, C₁₋₆        alkyl, C₁₋₆alkoxy, R^(a)R^(b)N—, R^(a)R^(b)N—SO₂— and        R^(a)R^(b)N-carbonyl-; wherein said C₁₋₆alkyl or C₁₋₆ alkoxy may        optionally be substituted by fluorine, hydroxyl or cyano; and        wherein the 4-7 membered heterocyclic ring may be optionally        substituted on nitrogen by one or more substituents selected        from the group consisting of C₁₋₆alkyl and        R^(a)R^(b)N-carbonyl-; and wherein said C₁₋₆alkyl may be        optionally substituted by fluorine, hydroxyl, cyano;

R^(P) may be independently selected, for each occurrence, from the groupconsisting of halogen, hydroxyl, cyano, C₁₋₆alkoxy, R^(i)R^(j)N—,R^(i)R^(j)N-carbonyl-, R^(i)R^(j)N—SO₂— andR^(i)R^(j)N-carbonyl-N(R^(a))—;

and pharmaceutically acceptable salts, stereoisomers, esters andprodrugs thereof.

In some embodiments, X¹ may be selected from the group consisting of:⁺—O—*, ⁺—N(R^(N1))—*, ⁺—C(R^(D1)R^(D2))—C(R^(D5)R^(D6))—*,⁺—C(R^(C1))═C(R^(C2))—*, ⁺—O—C(R^(D5)R^(D6))—*,⁺—N(R^(N2))—C(R^(D5)R^(D6))—*, ⁺—O—C(O)—*, ⁺—N(R^(N2))—C(O)—*,⁺—N═C(R^(C2))—* and ⁺—O—C(R^(D3)R^(D4))—C(R^(D5)R^(D6))—*; wherein theand * indicate the attachment points of X¹ as indicated in Formula I.Exemplary X¹ moities may be selected from the group consisting of:⁺—NH—*, ⁺—O—CH₂—*, ⁺—NH—CH₂—*, ⁺—N═CH—* and ⁺—CH═CH—*; wherein the ⁺and * indicate the attachment points of X¹ as indicated in Formula I.

In some embodiments X² may be selected from the group consisting of⁺—O—*, ⁺—N(R^(N1))—*, ⁺—C(R^(D1)R^(D2))—C(R^(D5)R^(D6))—*,⁺—O—C(R^(D5)R^(D6))—*, ⁺—N(R^(N2))—C(R^(D5)R^(D6))—*, ⁺—O—C(O)—*,⁺—N(R^(N2))—C(O)—*, and ⁺—O—C(R^(D3)R^(D4))—C(R^(D5)R^(D6))—*; whereinthe ⁺ and * indicate the attachment points of X² as indicated in FormulaII. Exemplary X² moities may be selected from the group consisting of:⁺—O—CH₂—* and ⁺—NH—CH₂—*; wherein the ⁺ and * indicate the attachmentpoints of X² as indicated in Formula II.

In one embodiment, R^(D1), R^(D2), R^(C1), R^(N1) and R^(N2) may beindependently selected for each occurrence from the group consisting ofhydrogen and methyl. For example, R^(D1), R^(D2)R^(C1), R^(N1) andR^(N2) may be hydrogen.

In certain embodiments, R^(D3), R^(D4), R^(D5) and R^(D6) may beindependently selected for each occurrence from the group consisting ofhydrogen, fluorine, cyano and C₁₋₂alkyl. For example, R^(D3), R^(D4),R^(D5) and R^(D6) may be hydrogen.

In an embodiment, R^(C2) may be selected from the group consisting ofhydrogen, halogen, cyano and C₁₋₂alkyl. For example, R^(C2) may behydrogen.

In certain embodiments, R^(B1) of the tricyclic compound of Formula IImay be selected from the group consisting of H, F or C₁₋₂alkyl. Forexample, R^(B1) may be H or methyl.

In another embodiment, R^(B2) of the tricyclic compound of Formula IImay be hydrogen.

In certain embodiments, ring D¹ may be selected from the groupconsisting of:

wherein the *, # and + indicate the points of attachment to the phenylring and the B¹ ring as indicated in Formula I. Exemplary D¹ rings thatmay form part of the contemplated tricyclic core may include thoseselected from the group consisting of:

In certain embodiments, ring D² may be selected from the groupconsisting of:

wherein the *, # and + indicate the points of attachment to the phenylring and the B² ring as indicated in Formula II.

In some embodiments, Y may be selected from the group consisting of abond, *—O—CH₂—^(#) and *—CH₂—O—CH₂—^(#); wherein the * and # indicatethe points of attachment to Y as indicated in Formula I or Formula II.For example, Y may be a bond or *—O—CH₂—^(#); wherein the * and #indicate the points of attachment to Y as indicated in Formula I orFormula II.

For example, ring B¹ or B² may, in certain embodiments, be selected fromthe group consisting of:

wherein the * and # indicate the points of attachment to Y as indicatedin Formula I and II. Exemplary B¹ and B² rings that may form part of thecontemplated tricyclic core may include those selected from the groupconsisting of:

Provided herein, for example, are tricyclic compounds represented byformulas Ia, Ib, Ic, Id, Ie, If and Ig:

In certain embodiments, A may be phenyl.

Also provided herein is a compound represented by Formula III:

wherein:

B¹ may be a 3-6 membered saturated or partially unsaturated heterocyclicor carbocyclic ring; wherein the ring B¹ may optionally be substitutedby one or more fluorine atoms on any of the available carbon atoms;

D¹ may be a 5-7 membered heterocyclic, carbocyclic, heteroaromatic oraromatic ring; wherein B¹ is fused to D¹ such that the two atoms sharedby B¹ and D¹ are both carbon; and wherein the bond common to both the B¹and D¹ rings may be a single or double bond;

X¹ may be selected from the group consisting of: ⁺—C(R^(D1)R^(D2))—*,⁺—W¹—*, ⁺—C(R^(D1)R^(D2))—C(R^(D5)R^(D6))—*, ⁺—C(R^(C1))═C(R^(C2))—*,⁺—W²—C(R^(D5)R^(D6))—*, ⁺—W²—C(O)—*, ⁺—C(R^(D1)R^(D2))—W⁴—*,⁺—N═C(R^(C2))—*, ⁺—C(R^(C1))═N—*,⁺—C(R^(D1)R^(D2))—C(R^(D3)R^(D4))—C(R^(D5)R^(D6))—*,⁺—W²—C(R^(D3)R^(D4))—C(R^(D5)R^(D6))—*, ⁺—W²—C(O)—C(R^(D5)R^(D6))—*,⁺—C(R^(D1)R^(D2))—W³—C(R^(D5)R^(D6))—*, ⁺—C(R^(D1)R^(D2))—W³—C(O)—*,⁺—C(R^(D1)R^(D2))—C(R^(D3)R^(D4))—W⁴—* and ⁺—C(R^(D1)R^(D2))—C(O)—W⁴—*;wherein the ⁺ and * indicate the attachment points of X¹ as indicated inFormula III;

Y may be selected from the group consisting of: a bond, *—CH₂—^(#),*—O—^(#), *—CH₂—CH₂—^(#), *—O—CH₂—^(#), *—CH₂—O—^(#),*—CH₂—CH₂—CH₂—^(#), *—O—CH₂—CH₂—^(#) and *—CH₂—O—CH₂—^(#); wherein the *and ^(#) indicate the attachment points of Y as indicated in FormulaIII;

W¹ may be selected from the group consisting of O, S or N(R^(N1));

W² may be selected from the group consisting of O or N(R^(N2));

W³ may be selected from the group consisting of O or N(R^(N3));

W⁴ may be selected from the group consisting of O or N(R^(N4));

R^(A1) may be selected, independently for each occurrence, from thegroup consisting of hydrogen, hydroxyl, cyano, halogen, C₁₋₄alkyl orC₁₋₃alkoxy; wherein C₁₋₄alkyl, or C₁₋₃alkoxy may be optionallysubstituted by one or more fluorines;

n may be 0, 1, or 2;

R^(A2) may be selected from the group consisting of hydrogen,R^(i)R^(j)N—, heterocyclyl, heterocyclyloxy and heterocyclyl-(NR^(a))—;wherein said heterocyclyl may optionally be substituted by one or moresubstituents selected from R^(g) and wherein if said heterocyclylcontains a —NH moiety that nitrogen may optionally be substituted by oneor more groups R^(h); or

R^(A2) may be selected from the group consisting of: C₁₋₆alkyl,C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy, C₃₋₆alkenyloxy,C₃₋₆alkynyloxy, C₃₋₆cycloalkoxy, C₁₋₆alkyl-S(O)_(w)— (wherein w is 0, 1or 2), C₁₋₆alkyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))-carbonyl-,C₁₋₆alkylcarbonyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))-carbonyl-N(R^(a))—,C₁₋₆alkyl-N(R^(a))—SO₂—, C₁₋₆alkyl-SO₂—N(R^(a))—,C₁₋₆alkoxycarbonyl-N(R^(a))—, C₁₋₆alkylcarbonyl-N(R^(a))—C₁₋₆alkyl-,C₁₋₆alkyl-N(R^(a))-carbonyl-C₁₋₆ alkyl-, C₁₋₆alkoxyC₁₋₆alkyl-; whereinC₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy,C₃₋₆alkenyloxy, C₃₋₆alkynyloxy, C₃₋₆cycloalkoxy, C₁₋₆alkyl-S(O)_(w)—,C₁₋₆alkyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))-carbonyl-,C₁₋₆alkylcarbonyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))-carbonyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))—SO₂—, C₁₋₆alkyl-SO₂—N(R^(a)), C₁₋₆alkoxycarbonyl(R^(a))—, C₁₋₆alkylcarbonyl-N(R^(a))C₁₋₆alkyl-,C₁₋₆alkyl-N(R^(a))-carbonyl-C₁₋₆alkyl-, C₁₋₆alkoxy-C₁₋₆alkyl mayoptionally be substituted by R^(P), phenyl, phenoxy, heteroaryl,heteroaryloxy, heteroaryl-(NR^(a))—, heterocyclyl, heterocyclyloxy orheterocyclyl-N(R^(a))—; and wherein said heteroaryl or phenyl mayoptionally be substituted with one or more substituents selected fromR^(f); and wherein said heterocyclyl may optionally be substituted byone or more substituents selected from R^(g); and wherein if saidheterocyclyl contains a —NH moiety that nitrogen may optionally besubstituted by one or more groups R^(h);

R^(D1) and R^(D2) may be each independently selected from the groupconsisting of hydrogen, fluorine, hydroxyl, C₁₋₂alkyl or C₁₋₂alkoxy;wherein the C₁₋₂alkyl and C₁₋₂alkoxy may optionally be substituted byone or more fluorine atoms or a group selected from cyano or hydroxyl;

R^(D3) and R^(D4) may be each independently selected from the groupconsisting of hydrogen, fluorine, hydroxyl, cyano, C₁₋₃alkyl orC₁₋₃alkoxy; wherein the C₁₋₃ alkyl and C₁₋₃ alkoxy may optionally besubstituted by one or more fluorine atoms or a group selected fromcyano, hydroxyl or N(R^(a)R^(b));

R^(D5) and R^(D6) may be each independently selected from the groupconsisting of hydrogen, fluorine, hydroxyl, cyano, C₁₋₂alkyl orC₁₋₂alkoxy; wherein the C₁₋₂alkyl and C₁₋₂ alkoxy may optionally besubstituted by one or more fluorine atoms or a group selected fromcyano, hydroxyl or N(R^(a)R^(b));

R^(C1) may be selected from the group consisting of hydrogen, halogen,C₁₋₂alkyl or C₁₋₂alkoxy; wherein the C₁₋₂alkyl or C₁₋₂alkoxy mayoptionally be substituted by one or more fluorine atoms;

R^(C2) may be selected from the group consisting of hydrogen, halogen,hydroxyl, cyano, C₁₋₂alkyl or C₁₋₂alkoxy; wherein the C₁₋₂alkyl andC₁₋₂alkoxy may optionally be substituted by one or more fluorine atomsor a group selected from cyano, hydroxyl or N(R^(a)R^(b));

R^(N1) may be selected from the group consisting of hydrogen orC₁₋₂alkyl;

R^(N2) may be selected from the group consisting of hydrogen orC₁₋₂alkyl;

R^(N3) may be selected from the group consisting of hydrogen, C₁₋₃alkylor C₁₋₂alkylcarbonyl; wherein the C₁₋₃alkyl and C₁₋₂alkylcarbonyl mayoptionally be substituted by one or more fluorine atoms or a groupselected from cyano, hydroxyl or N(R^(a)R^(b));

R^(N4) may be selected from the group consisting of hydrogen, C₁₋₃alkylor C₁₋₂ alkylcarbonyl; wherein the C₁₋₃alkyl and C₁₋₂alkylcarbonyl mayoptionally be substituted by one or more fluorine atoms or a groupselected from cyano, hydroxyl or N(R^(a)R^(b));

R^(a) and R^(b) may be independently selected, for each occurrence, fromthe group consisting of hydrogen and C₁₋₃alkyl; wherein C₁₋₃alkyl mayoptionally be substituted by one or more substituents selected fromfluorine, cyano, oxo and hydroxyl;

or R^(a) and R^(b), together with the nitrogen to which they areattached, may form a 4-6 membered heterocyclic ring, which may have anadditional heteroatom selected from O, S, or N; wherein the 4-6 memberedheterocyclic ring may optionally be substituted by one or moresubstituents selected from the group consisting of fluorine, cyano, oxoor hydroxyl;

R^(f) may be independently selected, for each occurrence, from the groupconsisting of R^(P), hydrogen, C₁₋₆alkyl, C₃₋₆cycloalkyl, C₂₋₆alkenyl,C₂₋₆alkynyl, C₁₋₆alkoxy, C₁₋₆alkyl-S(O)_(w)—, (wherein w is 0, 1 or 2),C₁₋₆alkylcarbonyl-N(R^(a))— and C₁₋₆alkoxycarbonyl-N(R^(a))—; whereinC₁₋₆alkyl, C₃₋₆cycloalkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₁₋₆alkoxy,C₁₋₆alkyl-S(O)_(w)—, C₁₋₆ alkylcarbonyl-N(R^(a))—,C₁₋₆alkoxycarbonyl-N(R^(a))— may be optionally substituted by one ormore substituents selected from R^(P);

R^(g) may be independently selected for each occurrence from the groupconsisting of R^(P), hydrogen, oxo, C₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl,C₃₋₆cycloalkyl, C₁₋₆alkoxy, C₁₋₆alkyl-S(O)_(w)—, (wherein w is 0, 1 or2), C₁₋₆alkylcarbonyl-N(R^(a))— and C₁₋₆alkoxycarbonyl-N(R^(a))—;wherein C₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy,C₁₋₆alkyl-S(O)_(w)—, C₁₋₆ alkylcarbonyl-N(R^(a))—,C₁₋₆alkoxycarbonyl-N(R^(a))— may be optionally substituted by one ormore substituents selected from R^(P);

R^(h) may be independently selected for each occurrence from the groupconsisting of hydrogen, C₁₋₆alkyl, C₃₋₆alkenyl, C₃₋₆alkynyl,C₃₋₆cycloalkyl, C₁₋₆alkyl-S(O)₂—, C₁₋₆alkoxycarbonyl-,R^(i)R^(j)N-carbonyl- and R^(i)R^(j)N—SO₂—; wherein C₁₋₆alkyl,C₃₋₆alkenyl, C₃₋₆alkynyl C₃₋₆cycloalkyl and C₁₋₆alkyl-S(O)₂—,C₁₋₆alkylcarbonyl- may optionally be substituted by one or moresubstituents selected from R^(P);

R^(i) and R^(j) may be selected independently for each occurrence fromthe group consisting of hydrogen, C₁₋₄alkyl C₃₋₆cycloalkyl, heterocyclyland heterocyclylcarbonyl; wherein C₁₋₄alkyl and C₃₋₆cycloalkyl may beoptionally substituted by one or more substituents selected fromfluorine, hydroxyl, cyano, R^(a)R^(b)N—, R^(a)R^(b)N-carbonyl- andC₁₋₃alkoxy and wherein heterocyclyl and heterocyclylcarbonyl may beoptionally substituted by one or more substituents selected fromC₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy,halo-C₁₋₆-alkyl, hydroxyl-C₁₋₆-alkyl, R^(a)R^(b)N—C₁₋₆alkyl- andC₁₋₆-alkoxy-C₁₋₆-alkyl group; and wherein if said heterocyclyl orheterocyclylcarbonyl contains a —NH moiety that nitrogen may optionallybe substituted by one or more groups C₁₋₆alkyl, C₃₋₆alkenyl,C₃₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkyl-S(O)₂— and C₁₋₆-alkylcarbonyl;

or R^(i) and R^(j) taken together with the nitrogen to which they areattached may form a 4-7 membered heterocyclic ring, which may have anadditional heteroatom selected from O, S, or N; wherein the 4-7 memberedheterocyclic ring may be optionally substituted on carbon by one or moresubstituents selected from the group consisting of fluorine, hydroxyl,oxo, cyano, C₁₋₆ alkyl, C₁₋₆alkoxy, R^(a)R^(b)N—, R^(a)R^(b)N—SO₂— andR^(a)R^(b)N-carbonyl-; wherein said C₁₋₆alkyl or C₁₋₆alkoxy mayoptionally be substituted by fluorine, hydroxyl or cyano; and whereinthe 4-7 membered heterocyclic ring may be optionally substituted onnitrogen by one or more substituents selected from the group consistingof C₁₋₆alkyl and R^(a)R^(b)N-carbonyl-; and wherein said C₁₋₆alkyl maybe optionally substituted by fluorine, hydroxyl, cyano;

R^(P) may be independently selected, for each occurrence, from the groupconsisting of halogen, hydroxyl, cyano, C₁₋₆alkoxy, R^(i)R^(j)N—,R^(i)R^(j)N-carbonyl-, R^(i)R^(j)N—SO₂— andR^(i)R^(j)N-carbonyl-N(R^(a))—;

and pharmaceutically acceptable salts, stereoisomers, esters andprodrugs thereof.

In certain embodiments, R^(A1) of the tricyclic compound of Formula IIImay be selected from the group consisting of hydrogen, halogen,C₁₋₂alkyl and C₁₋₂alkoxy; wherein C₁₋₂ alkyl may optionally besubstituted by one or more fluorines. For example, R^(A1) may behydrogen or fluorine.

In another embodiment, R^(A2) of the tricyclic compound of Formula IIImay be selected from the group consisting of hydrogen, R^(i)R^(j)N,heterocyclyl, C₁₋₆alkyl, C₃₋₆alkenyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy;wherein said heterocyclyl may optionally be substituted by one or moregroups R^(g); and wherein if said heterocyclyl contains a —NH moiety,that nitrogen may optionally be substituted by on or more groups R^(h);and wherein said C₁₋₆alkyl, C₃₋₆alkenyl, C₃₋₆cycloalkyl and C₁₋₆alkoxymay optionally be substituted by one or more groups R^(P). For example,R^(A2) may be selected from the group consisting of3-(N,N-diethylamino)propyl, 3-(pyrrolidin-1-yl)propyl,(Z)-3-(N,N-diethylamino)prop-1-enyl, (Z)-3-(azetidin-1-yl)prop-1-enyland (Z)-3-(pyrrolidin-1-yl)prop-1-enyl.

Also provided herein is a compound represented by Formula IV:

D² may be a 5-7 membered partially unsaturated heterocyclic orcarbocyclic ring;

X² may be selected from the group consisting of: ⁺—C(R^(D1)R^(D2))—*,⁺—W¹—*, ⁺—C(R^(D1)R^(D2))—C(R^(D5)R^(D6))—*, ⁺—W²—C(R^(D5)R^(D6))—*,⁺—W²—C(O)—*, ⁺—C(R^(D1)R^(D2))—W⁴—*,⁺—C(R^(D1)R^(D2))—C(R^(D3)R^(D4))—C(R^(D5)R^(D6))—*,⁺—W²—C(R^(D3)R^(D4))—C(R^(D5)R^(D6))—*, ⁺—W²—C(O)—C(R^(D5)R^(D6))—*,⁺—C(R^(D1)R^(D2))—W³—C(R^(D5)R^(D6))—*, ⁺—C(R^(D1)R^(D2))—W³—C(O)—*,⁺—C(R^(D1)R^(D2))—C(R^(D3)R^(D4))—W⁴—* and ⁺—C(R^(D1)R^(D2))—C(O)—W⁴—*;wherein the ⁺ and * indicate the attachment points of X² as indicated inFormula IV;

W¹ may be selected from the group consisting of O, S or N(R^(N1));

W² may be selected from the group consisting of O or N(R^(N2));

W³ may be selected from the group consisting of O or N(R^(N3));

W⁴ may be selected from the group consisting of O or N(R^(N4));

R^(B1) may be selected from the group consisting of H, F, OH, CN,C₁₋₂alkoxy or C₁₋₃ alkyl; wherein C₁₋₃alkyl and C₁₋₂alkoxy areoptionally substituted by a group selected from OH, C₁₋₂alkoxy, CN orone or more fluorine atoms;

R^(A1) may be selected, independently for each occurrence, from thegroup consisting of hydrogen, hydroxyl, cyano, halogen, C₁₋₄alkyl orC₁₋₃alkoxy; wherein C₁₋₄alkyl, or C₁₋₃alkoxy may be optionallysubstituted by one or more fluorines;

n may be 0, 1, or 2;

R^(A2) may be selected from the group consisting of hydrogen,R^(i)R^(j)N—, heterocyclyl, heterocyclyloxy and heterocyclyl-(NR^(a))—;wherein said heterocyclyl may optionally be substituted by one or moresubstituents selected from R^(g) and wherein if said heterocyclylcontains a —NH moiety that nitrogen may optionally be substituted by oneor more groups R^(h); or

R^(A2) may be selected from the group consisting of: C₁₋₆alkyl,C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy, C₃₋₆alkenyloxy,C₃₋₆alkynyloxy, C₃₋₆cycloalkoxy, C₁₋₆alkyl-S(O)_(w)— (wherein w is 0, 1or 2), C₁₋₆alkyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))-carbonyl-,C₁₋₆alkylcarbonyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))-carbonyl-N(R^(a))—,C₁₋₆alkyl-N(R^(a))—SO₂—, C₁₋₆alkyl-SO₂—N(R^(a))—,C₁₋₆alkoxycarbonyl-N(R^(a))—, C₁₋₆alkylcarbonyl-N(R^(a))—C₁₋₆alkyl-,C₁₋₆alkyl-N(R^(a))-carbonyl-C₁₋₆ alkyl-, C₁₋₆alkoxyC₁₋₆alkyl-; whereinC₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆ alkoxy,C₃₋₆alkenyloxy, C₃₋₆alkynyloxy, C₃₋₆cycloalkoxy, C₁₋₆alkyl-S(O)_(w)—,C₁₋₆alkyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))-carbonyl-,C₁₋₆alkylcarbonyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))-carbonyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))—SO₂—, C₁₋₆alkyl-SO₂—N(R^(a)), C₁₋₆alkoxycarbonyl(R^(a))—, C₁₋₆alkylcarbonyl-N(R^(a))C₁₋₆alkyl-,C₁₋₆alkyl-N(R^(a))-carbonyl-C₁₋₆alkyl-, C₁₋₆alkoxy-C₁₋₆alkyl mayoptionally be substituted by R^(P), phenyl, phenoxy, heteroaryl,heteroaryloxy, heteroaryl-(NR^(a))—, heterocyclyl, heterocyclyloxy orheterocyclyl-N(R^(a))—; and wherein said heteroaryl or phenyl mayoptionally be substituted with one or more substituents selected fromR^(f); and wherein said heterocyclyl may optionally be substituted byone or more substituents selected from R^(g); and wherein if saidheterocyclyl contains a —NH moiety that nitrogen may optionally besubstituted by one or more groups R^(h);

R^(D1) and R^(D2) may be each independently selected from the groupconsisting of hydrogen, fluorine, hydroxyl, C₁₋₂alkyl or C₁₋₂alkoxy;wherein the C₁₋₂alkyl and C₁₋₂alkoxy may optionally be substituted byone or more fluorine atoms or a group selected from cyano or hydroxyl;

R^(D3) and R^(D4) may be each independently selected from the groupconsisting of hydrogen, fluorine, hydroxyl, cyano, C₁₋₃alkyl orC₁₋₃alkoxy; wherein the C₁₋₃ alkyl and C₁₋₃ alkoxy may optionally besubstituted by one or more fluorine atoms or a group selected fromcyano, hydroxyl or N(R^(a)R^(b));

R^(D5) and R^(D6) may be each independently selected from the groupconsisting of hydrogen, fluorine, hydroxyl, cyano, C₁₋₂alkyl orC₁₋₂alkoxy; wherein the C₁₋₂alkyl and C₁₋₂ alkoxy may optionally besubstituted by a substituent or substituents selected from the groupconsisting of: one or more fluorine atoms, cyano, hydroxyl orN(R^(a)R^(b));

R^(C1) may be selected from the group consisting of hydrogen, halogen,C₁₋₂alkyl or C₁₋₂ alkoxy; wherein the C₁₋₂alkyl or C₁₋₂alkoxy mayoptionally be substituted by one or more fluorine atoms;

R^(C2) may be selected from the group consisting of hydrogen, halogen,hydroxyl, cyano, C₁₋₂alkyl or C₁₋₂alkoxy; wherein the C₁₋₂alkyl andC₁₋₂alkoxy may optionally be substituted by one or more fluorine atomsor a group selected from cyano, hydroxyl or N(R^(a)R^(b));

R^(N1) may be selected from the group consisting of hydrogen orC₁₋₂alkyl;

R^(N2) may be selected from the group consisting of hydrogen orC₁₋₂alkyl;

R^(N3) may be selected from the group consisting of hydrogen, C₁₋₃alkylor C₁₋₂ alkylcarbonyl; wherein the C₁₋₃alkyl and C₁₋₂alkylcarbonyl mayoptionally be substituted by a substituent or substituents selected fromthe group consisting of: one or more fluorines, cyano, hydroxyl orN(R^(a)R^(b));

R^(N4) may be selected from the group consisting of hydrogen, C₁₋₃alkylor C₁₋₂ alkylcarbonyl; wherein the C₁₋₃alkyl and C₁₋₂alkylcarbonyl mayoptionally be substituted by a substituent or substituents selected fromthe group consisting of: one or more fluorines, cyano, hydroxyl orN(R^(a)R^(b));

R^(a) and R^(b) may be independently selected, for each occurrence, fromthe group consisting of hydrogen and C₁₋₃alkyl; wherein C₁₋₃alkyl mayoptionally be substituted by one or more substituents selected fromfluorine, cyano, oxo and hydroxyl;

or R^(a) and R^(b), together with the nitrogen to which they areattached, may form a 4-6 membered heterocyclic ring, which may have anadditional heteroatom selected from O, S, or N; wherein the 4-6 memberedheterocyclic ring may optionally be substituted by one or moresubstituents selected from the group consisting of fluorine, cyano, oxoor hydroxyl;

R^(f) may be independently selected, for each occurrence, from the groupconsisting of R^(P), hydrogen, C₁₋₆alkyl, C₃₋₆cycloalkyl, C₂₋₆alkenyl,C₂₋₆alkynyl, C₁₋₆alkoxy, C₁₋₆alkyl-S(O)_(w)—, (wherein w is 0, 1 or 2),C₁₋₆alkylcarbonyl-N(R^(a))— and C₁₋₆alkoxycarbonyl-N(R^(a))—; whereinC₁₋₆alkyl, C₃₋₆cycloalkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₁₋₆alkoxy,C₁₋₆alkyl-S(O)_(w)—, C₁₋₆ alkylcarbonyl-N(R^(a))—,C₁₋₆alkoxycarbonyl-N(R^(a))— may be optionally substituted by one ormore substituents selected from R^(P);

R^(g) may be independently selected for each occurrence from the groupconsisting of R^(P), hydrogen, oxo, C₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl,C₃₋₆cycloalkyl, C₁₋₆alkoxy, C₁₋₆alkyl-S(O)_(w)—, (wherein w is 0, 1 or2), C₁₋₆alkylcarbonyl-N(R^(a))— and C₁₋₆alkoxycarbonyl-N(R^(a))—;wherein C₁₋₆ alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl,C₁₋₆alkoxy, C₁₋₆alkyl-S(O)_(w)—, C₁₋₆ alkylcarbonyl-N(R^(a))—,C₁₋₆alkoxycarbonyl-N(R^(a))— may be optionally substituted by one ormore substituents selected from R^(P);

R^(h) may be independently selected for each occurrence from the groupconsisting of hydrogen, C₁₋₆alkyl, C₃₋₆alkenyl, C₃₋₆alkynyl,C₃₋₆cycloalkyl, C₁₋₆alkyl-S(O)₂—, C₁₋₆ alkoxycarbonyl-,R^(i)R^(j)N-carbonyl- and R^(i)R^(j)N—SO₂—; wherein C₁₋₆alkyl,C₃₋₆alkenyl, C₃₋₆alkynyl C₃₋₆cycloalkyl and C₁₋₆alkyl-S(O)₂—,C₁₋₆alkylcarbonyl- may optionally be substituted by one or moresubstituents selected from R^(P);

R^(i) and R^(j) may be selected independently for each occurrence fromthe group consisting of hydrogen, C₁₋₄alkyl C₃₋₆cycloalkyl, heterocyclyland heterocyclylcarbonyl; wherein C₁₋₄alkyl and C₃₋₆cycloalkyl may beoptionally substituted by one or more substituents selected fromfluorine, hydroxyl, cyano, R^(a)R^(b)N—, R^(a)R^(b)N-carbonyl- andC₁₋₃alkoxy and wherein heterocyclyl and heterocyclylcarbonyl may beoptionally substituted by one or more substituents selected fromC₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy,halo-C₁₋₆-alkyl, hydroxyl-C₁₋₆-alkyl, R^(a)R^(b)N—C₁₋₆alkyl- andC₁₋₆-alkoxy-C₁₋₆-alkyl group; and wherein if said heterocyclyl orheterocyclylcarbonyl contains a —NH moiety that nitrogen may optionallybe substituted by one or more groups C₁₋₆alkyl, C₃₋₆alkenyl,C₃₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkyl-S(O)₂— and C₁₋₆-alkylcarbonyl;

or R^(i) and R^(j) taken together with the nitrogen to which they areattached may form a 4-7 membered heterocyclic ring, which may have anadditional heteroatom selected from O, S, or N; wherein the 4-7 memberedheterocyclic ring may be optionally substituted on carbon by one or moresubstituents selected from the group consisting of fluorine, hydroxyl,oxo, cyano, C₁₋₆ alkyl, C₁₋₆alkoxy, R^(a)R^(b)N—, R^(a)R^(b)N—SO₂— andR^(a)R^(b)N-carbonyl-; wherein said C₁₋₆alkyl or C₁₋₆ alkoxy mayoptionally be substituted by fluorine, hydroxyl or cyano; and whereinthe 4-7 membered heterocyclic ring may be optionally substituted onnitrogen by one or more substituents selected from the group consistingof C₁₋₆alkyl and R^(a)R^(b)N-carbonyl-; and wherein said C₁₋₆alkyl maybe optionally substituted by one or more substituents selected from thegroup consisting of fluorine, hydroxyl, cyano;

R^(P) may be independently selected, for each occurrence, from the groupconsisting of halogen, hydroxyl, cyano, C₁₋₆alkoxy, R^(i)R^(j)N—,R^(i)R^(j)N-carbonyl-, R^(i)R^(j)N—SO₂— andR^(i)R^(j)N-carbonyl-N(R^(a))—;

and pharmaceutically acceptable salts, stereoisomers, esters andprodrugs thereof.

In certain embodiments, R^(A1) of the tricyclic compound of Formula IVmay be hydrogen or fluorine.

In another embodiment, R^(A2) of the tricyclic compound of Formula IVmay be selected from the group consisting of hydrogen, R^(i)R^(j)N,heterocyclyl, C₁₋₆alkyl, C₃₋₆alkenyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy,heterocyclyl-NR^(a)-carbonyl-C₁₋₆alkyl andheterocyclyl-carbonyl-NR^(a)—C₁₋₆alkyl; wherein said heterocyclyl mayoptionally be substituted by one or more groups R^(g); and wherein ifsaid heterocyclyl contains a —NH moiety, that nitrogen may optionally besubstituted by on or more groups R^(h); and wherein said C₁₋₆alkyl,C₃₋₆alkenyl, C₃₋₆cycloalkyl and C₁₋₆alkoxy may optionally be substitutedby one or more groups R^(P).

Also provided herein are compounds that may be selected from the groupconsisting of:cis-(3aRS,9bRS)-7-(benzenesulfonylamino)-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylicacid;cis-(3aRS,9bRS)-7-[2-(3-diethylaminopropyl)-4-fluorobenzenesulfonyl-amino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylicacid;cis-(3aRS,9bRS)-7-[2-(3-{pyrrolidin-1-yl}propyl)-4-fluorobenzenesulfonylamino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylicacid;cis-(3aRS,9bRS)-7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylicacid;cis-(3aR,9bR)-7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluoro-benzenesulfonylamino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylicacid;cis-(3aS,9bS)-7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylicacid;7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,2-dihydrofuro[2,3-c]quinoline-6-carboxylicacid formate salt;7-(benzenesulfonylamino))-1,2-dihydrofuro[2,3-c]quinoline-6-carboxylicacid formate salt;cis-(3aRS,9bRS)-7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,2,3a,4,5,9b-hexahydrofuro[2,3-c]quinoline-6-carboxylicacid;(1aRS,7bSR)-5-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aR,7bS)-5-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aS,7bR)-5-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-7b-methyl-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-[2-((E)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-7b-methyl-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;cis-(3aRS,9bRS)-7-[2-(4-dimethylamino-butylamino)-benzenesulfonylamino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylicacid;(1aR,7bS)-5-[2-(3-diethylaminopropyl)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzene-sulfonylamino]-1,1-difluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aR,7bS)-5-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzene-sulfonylamino]-1,1-difluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aS,7bR)-5-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzene-sulfonylamino]-1,1-difluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-[2((Z)-3-ethylaminoprop-1-enyl)-4-fluoro-benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid;(1aR,7bS)-5-[2((Z)-3-ethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aS,7bR)-5-[2((Z)-3-ethylaminoprop-1-enyl)-4-fluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2[(Z)-3-(pyrrolidin-1-yl)prop-1-enyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylicacid;(1aR,7bS)-5-{2[(Z)-3-(pyrrolidin-1-yl)prop-1-enyl]-4-fluorobenzenesulfonyl-amino}-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylicacid;(1aS,7bR)-5-{2[(Z)-3-(pyrrolidin-1-yl)prop-1-enyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-[2-(3-dimethylaminopropylamino)-benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid; (1aR,7bS)-5-[2-(3-dimethylaminopropylamino)benzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aS,7bR)-5-[2-(3-dimethylaminopropyl-amino)benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-[2-(4-dimethylaminobutylamino)benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aR,7bS)-5-[2-(4-dimethylamino-butylamino)benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aS,7bR)-5-[2-(4-dimethylaminobutylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-[2-(5-dimethylamino-pentylamino)benzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2[(Z)-3-(propan-2-yl)aminoprop-1-enyl]-4-fluorobenzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2[(Z)-3-((S)-3-hydroxypyrrolidin-1-yl)aminoprop-1-enyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2[(Z)-3-((R)-3-hydroxypyrrolidin-1-yl)aminoprop-1-enyl]-4-fluorobenzene-sulfonylamino}-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-[2((Z)-4-diethylaminobut-1-enyl)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aR,7bS)-5-[2((Z)-4-diethylaminobut-1-enyl)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid; (1aS,7bR)-5-[2((Z)-4-diethylaminobut-1-enyl)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2-[2-(4-ethylpiperazin-1-yl)-ethyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2[(Z)-3-(azetidin-1-yl)prop-1-enyl]-4-fluorobenzene-sulfonylamino}-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2[(Z)-3-(3-hydroxy-azetidin-1-yl)prop-1-enyl]-4-fluorobenzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2[(Z)-3-(azetidin-1-yl)propyl]-4-fluorobenzenesulfonylamino)}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-[2((Z)-4-diethylaminobutyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2-[N-(4-dimethylaminobutyl)-N-methylamino]-benzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2-[((S)-1-ethylpyrrolidin-3-ylcarbamoyl)-methyl]-4-fluoro-benzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-[2-(1-ethylazetidin-3-yl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2-[((R)-1-ethylpyrrolidin-3-ylcarbamoyl)methyl]-4-fluorobenzenesulfonyl-amino}-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2-[2-(pyrrolidin-1-yl)-ethyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-[2-((R)-1-ethylpyrrolidin-3-ylmethyl)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylicacid;(1aS,7bR)-5-[2-((R)-1-ethylpyrrolidin-3-ylmethyl)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylicacid; (1aR,7bS)-5-[2-((R)-1-ethylpyrrolidin-3-ylmethyl)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2-[((S)-1-ethylpyrrolidin-2-yl)cabonyl-aminomethyl]-4-fluorobenzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-[2-(4-dimethylaminobutyrylamino)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-[2-((S)-1-ethyl-pyrrolidin-3-ylmethyl)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-[2-(3-dimethylaminopropylcarbamoyl)benzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-(2-{[N—((S)-1-ethyl-pyrrolidin-3-yl)-N-methylcarbamoyl]methyl}-4-fluoro-benzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-(2-{[N—((R)-1-ethyl-pyrrolidin-3-yl)-N-methylcarbamoyl]methyl}-4-fluoro-benzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2-[2-((S)-1-ethylpyrrolidin-2-yl)ethylamino]-benzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2-[2-((R)-1-ethylpyrrolidin-2-yl)ethylamino]-benzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-[2-(3-N,N,-diethylaminopropylamino)benzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-(2-{[((R)-1-ethylpyrrolidine-2-yl)carbonyl-amino]methyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2-[(1-ethylazetidin-3-ylmethyl)amino]benzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid; (1aS,7bR)-5-[2-((Z)-3-diethylaminoprop-1-enyl)benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aR,7bS)-5-[2-((Z)-3-diethylaminoprop-1-enyl)benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-(2-{N—[((R)-1-ethylpyrrolidine-2-yl)carbonyl]-N-methyl-aminomethyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-(2-{N—[((S)-1-ethylpyrrolidine-2-yl)carbonyl]-N-methylamino-methyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-[2-(4-dimethylaminobutylamino)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2-[((R)-1-ethylpyrrolidin-3-ylmethyl)amino]-benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2-[((S)-1-ethylpyrrolidin-3-ylmethyl)amino]-benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-[2-(4-ethyl-2-oxopiperazin-1-ylmethyl)-4-fluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-[2-(1-ethylpiperidin-4-ylmethyl)-4-fluoro-benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2-[2-(1-ethylazetidin-3-yl)ethyl]-4-fluoro-benzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2-[((S)-1-azabicyclo[2.2.2]oct-3-yl)amino]benzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2-[((R)-1-azabicyclo-[2.2.2]oct-3-yl)amino]benzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-(2-{[((S)-1-ethylpyrrolidine-3-carbonyl)amino]methyl}-4-fluoro-benzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2-[2-((R)-1-ethylpyrrolidin-3-ylamino)ethyl]-4-fluoro-benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2-[((R)-1-ethylpyrrolidin-3-yl)amino]-benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2-[((S)-1-ethylpyrrolidin-3-yl)amino]-benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-(2-{[((R)-1-ethylpyrrolidine-3-carbonyl)amino]-methyl)}-4-fluoro-benzenesulfonylamino)-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-[2-((Z)-3-diethylamino-2-methylprop-1-enyl)-4-fluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2-[2-((R)-1-ethylpyrrolidin-3-yl)ethylamino]-benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid;(1aRS,7bSR)-5-{2-[2-((S)-1-ethylpyrrolidin-3-yl)ethylamino]-benzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid;(1aR,7bS)-5-[2-((S)-1-ethylpyrrolidin-3-yloxymethyl)-4-fluoro-benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid; (1aR,7bS)-5-[2-((R)-1-ethylpyrrolidin-3-yloxymethyl)-4-fluoro-benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid;(1aR,7bS)-5-[2-(1-ethylpiperidin-3-ylmethyl)-4-fluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid;(1aR,7bS)-5-{2-[2-((R)-1-ethylpyrrolidin-2-yl)ethyl]-4-fluorobenzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid; and pharmaceutically acceptable salts, stereoisomers, esters andprodrugs thereof.

Procedures for making compounds described herein are provided below withreference to Schemes 1-3. In the reactions described below, it may benecessary to protect reactive functional groups (such as hydroxyl,amino, thio or carboxyl groups) to avoid their unwanted participation inthe reactions. The incorporation of such groups, and the methodsrequired to introduce and remove them are known to those skilled in theart (for example, see Greene, Wuts, Protective Groups in OrganicSynthesis. 2nd Ed. (1999)). The deprotection step may be the final stepin the synthesis such that the removal of protecting groups affordscompounds of Formula I, as disclosed herein, or as exemplified in, forexample, General Formula I, below. Starting materials used in thefollowing schemes can be purchased or prepared by methods described inthe chemical literature, or by adaptations thereof, using methods knownby those skilled in the art. The order in which the steps are performedcan vary depending on the groups introduced and the reagents used, butwould be apparent to those skilled in the art.

The general synthetic strategy used to prepare the tricyclic compoundsof General Formula I is depicted in Scheme 1. The tricyclic system maybe assembled in a variety of ways, starting from an appropriatelysubstituted and protected phenyl ring 1A. The group G′ is a suitablyprotected carboxylic acid, such as a methyl- or t-butyl carboxylate oris a functional group that may be readily converted into a carboxylicacid, such as a nitrile or aldehyde. The group G is a sulfonamide group,or a functional group that may be subsequently converted into asulfonamide group such as a suitably protected aniline. The B′-ring canbe directly attached to the substituted phenyl ring to give intermediate1B, and then the D′-ring can be formed by an intra-molecular reaction togive intermediate 1E. Alternatively, the B′-ring can be attached to thesubstituted phenyl ring 1A via a linker, X′, to give intermediate 1C,and then the D′-ring can be formed by an intra-molecular reaction togive intermediate 1E. Alternatively, the D′-ring can be built up ontothe substituted phenyl ring to give intermediate 1D, and then theB′-ring assembled to give intermediate 1E. Modifications to the B′ andD′ rings may be necessary to provide the required saturated or partiallyunsaturated ring systems and this may be carried out prior to theformation of the tricyclic core or after it. For example, if the B′ ringis a dihydro- or tetrahydrofuran it may be prepared from a correspondingfuran compound by hydrogenation in the presence of a metal catalyst (forexample palladium or palladium hydroxide on a solid support such ascarbon) in a solvent (such as ethyl acetate, ethanol or dioxane)optionally in the presence of an acid (such as acetic acid). Thehydrogenation may be carried out at any stage during the synthesis ofthe compounds either before or after the formation of the tricycliccore. Compounds of Formula I can be prepared from intermediate 1E byremoval of any protecting groups. Alternatively, further modificationsmay be made to 1E, such as modifications at G, before the removal of anyprotecting groups to give compounds of General Formula I. Specific stepsin the synthetic process are described in more detail below.

In Scheme 1, Step (i), compounds of structure 1A may be coupled under arange of conditions to compounds of structure 1B′, where B′ is anappropriate ring to afford compounds of the type 1B. The introduction ofthe B′ ring may require a number of steps and the preparation of anumber of intermediates. Protecting groups may also be required. If R¹is a suitable group (such as a halide or triflate), 1B′ can be convertedto 1B by formation of a carbon-carbon bond. The carbon-carbon bond canbe formed by reacting compounds of structure 1B′ where R³ is a borane,boronate or boronic acid group (such as a 2-formylfuran-3-boronate) inthe presence of a palladium catalyst (such as palladium chloride dppf ortris-(dibenzylideneacetone)-dipalladium), in the presence of a base(such as cesium carbonate) and a suitable reagent (such as a phosphine,for example, tri-tert-butyl-phosphonium tetrafluoroborate ortriphenylphosphine) in an appropriate solvent (such as dioxane, water ortetrahydrofuran, or mixtures thereof) and under appropriate conditions(such as heating, for example heating at 80-120° C. for 1-2 hours ormicrowave irradiation at 120-160° C. for 10 minutes to 1 hour) to afford1B. A wide range of appropriate reagents and conditions are known tothose skilled in the art to couple organoboranes, boronates and boronicacids to compounds such as 1A. [For example, see Miyaura, Suzuki, Chem.Rev. 1995, 95, 2457; Suzuki, Modern Arene Chemistry 2002, 53-106].

Alternatively the carbon-carbon bond in Scheme 1, Step (i) can be formedby coupling compounds of structure 1B′ in which B′ is an appropriatering and where R³ is a trialkylstannane (such as a tri-n-butylstannane)with compounds of structure 1A where R¹ is a suitable group (such as ahalide of triflate) in the presence of a palladium catalyst (such aspalladium chloride dppf), in an appropriate solvent (such asdimethoxyethane or tetrahydrofuran) and under appropriate conditions(such as heating, at 80-120° C. for 1-2 hours or by microwaveirradiation at 120-160° C. for 10 minutes to 1 hour) to afford 1B. Awide range of appropriate reagents and conditions are known to thoseskilled in the art to couple stannanes to aryl halides such as 1A. [Forexample, see Smith, March, March's Advanced Organic Chemistry, 5^(th)Edition, Wiley: New York, 2001, pp. 931-932; De Souza, Current OrganicSynthesis 2006, 3(3), 313-326.].

Alternatively compounds of structure 1A, where R¹ is a suitable group(such as a halide or triflate), can be treated with, for example, adiboronate (such as bis-pinacolatodiboron) in the presence of apalladium catalyst (such as palladium chloride dppf) and a base (such aspotassium acetate or diisopropylamine) in an appropriate solvent (suchas a mixture of dioxane and water) and under appropriate conditions(such as heating, for example at 80-120° C. for 1-2 hours or bymicrowave irradiation at 120-160° C. for 10 minutes to 1 hour) to give acompound of structure 1A, where R¹ is a boronate. A wide range ofappropriate reagents and conditions are known to those skilled in theart to convert an aryl halide (or aryl triflate) to an arylboronate (oran arylborane) [for example, see Marshall Chemtracts 2000, 13(4),219-222]. The arylboronate (or arylborane) thus formed, can then betreated with compounds of structure 1B′ (where R³ is a halogen ortriflate) in the presence of suitable reagents such as a phosphine (forexample tri-tert-butyl-phosphonium tetrafluoroborate), a base (such ascesium carbonate) and a catalyst (such astris-(dibenzylideneacetone)-dipalladium) in an appropriate solvent (suchas a mixture of water and dioxane) under appropriate conditions (such asheating at 80-120° C. for 1-2 hours or by microwave irradiation at120-160° C. for 10 minutes to 1 hour) to afford compounds of structure1B.

In Scheme 1, Step (iv), the groups R² and R⁴ of compound 1B can becoupled together to give the group X′, which forms the D′-ring. R² or R⁴may have been masked by protecting groups during Step (i), and mayrequire deprotection before the group X′ can be formed. Alternatively,R² or R⁴ may require chemical modification before the group X′ can beformed. For example if R² or R⁴ is a nitro group, that group may bereduced, for example using hydrogen in the presence of a suitablecatalyst (such as palladium on a solid support, such as carbon); or bytreatment with an inorganic reducing agent (such as tin (II) chloride inDMF) to give an amino group. For example, if R² or R⁴ is a hydroxyalkylgroup, that group may be treated with an oxidising agent (such as Jonesreagent or manganese dioxide) to give an aldehyde; or with a differentoxidising agent (such as potassium permanganate) to give a carboxylicacid. For example, if R² or R⁴ is an aldehyde, that group may be treatedwith an oxidising agent (such as potassium permanganate) to give acarboxylic acid or with a reducing agent (such as sodium borohydride) togive an alcohol. For example, if R² or R⁴ is a ketone, that group may betreated with a reducing agent (such as sodium borohydride) to give asecondary alcohol. For example, if R² or R⁴ is a carboxylic acid orester, that group may be treated with a reducing agent (such as lithiumaluminium hydride) to give an alcohol. For example, if R² or R⁴ is analkene group, that group may be treated with a borane (such as9-borobicyclononane) and converted to a primary or secondary alcohol.

Formation of the linker X′ may be carried out in a number of ways knownto those skilled in the art. For example, if one of the two groups R²and R⁴ is a hydroxyl and the other is a substituted alkylalcohol then 1Bcan be treated with a dehydrating agent (such as diisopropylazodicarboxylate) in the presence of a phosphine, (such astriphenylphosphine) to give 1E, where X′ is an ether. Alternatively, ifone of the two groups R² or R⁴ is a hydroxyl and the other group is analkyl group substituted with a leaving group (such as a halogen,tosylate or triflate) 1B can be treated with a base (such asdiisopropylethylamine, potassium carbonate or sodium hydride) to form1E, where X′ is an ether.

Alternatively, if one of the groups R² or R⁴ is a carboxylic acid andthe other group is an alkyl halide or sulfonate, then 1B can be treatedwith a base such as diisopropylethylamine, potassium carbonate or sodiumhydride to form 1E, where X′ is an ester.

Alternatively, if one of the two groups R² or R⁴ is a hydroxyl, orsubstituted alkylalcohol and the other group is a carboxylic acid orcarboxylic ester, then 1B can be treated with an acid (such ashydrochloric acid) or dehydrating agent (such asdicyclohexylcarbodiimide or acetic anhydride) to form 1E, where X′ is anester.

Alternatively, if one of the two groups R² or R⁴ on 1B is a hydroxyl orsubstituted alkylalcohol and the other group is a carboxylic acid, thenthe carboxylic acid can first be converted to a mixed anhydride (forexample by treatment with 2,4,6-trichlorobenzoyl chloride) or to anactivated ester (for example by treatment with HATU in the presence of abase such as diisopropylethylamine or pyridine), and the resulting mixedanhydride or activated ester can be further treated with a base (such asdiisopropylethylamine, pyridine or potassium carbonate) to form 1E,where X′ is an ester.

Alternatively, if one of the groups R² or R⁴ on 1B is an amine or asubstituted alkylamine and the other group is a carboxylic acid, thecarboxylic acid can be converted to an activated ester (for example bytreatment with HATU and a base such as diisopropylethylamine or pyridineor TBTU in the presence of N-methylmorpholine), and the resultingactivated ester can be further treated with a base to form 1E where X′is an amide.

Alternatively, if one of the two groups R² or R⁴ on 1B is an amine, or asubstituted alkylamine and the other group is a carboxylic acid, then 1Bcan then be treated with a dehydrating agent (such as such asdiisopropylcarbodiimide) to form 1E, where X′ is an amide.

Alternatively, if one of the two groups R² or R⁴ is an amine, orsubstituted alkylamine and the other group is an alkyl group substitutedwith a leaving group (such as a halogen, tosylate or triflate) then 1Bcan be treated with a base (such as diisopropylethylamine, pyridine orpotassium carbonate) to form 1E, where X′ is a substituted amine.

Alternatively, if one of the two groups R² or R⁴ is an aldehyde, and theother group is a phosphorane (such as an alkyl triphenylphosphorane) oran alkyl phosphonate (such as an alkyl phosphonic acid diethyl ester)then 1B can be treated with a base (such as diisopropylethylamine,potassium carbonate or sodium hexamethyldisilazide) to form 1E, where X′is an alkene which may, or may not be further substituted.

Alternatively, if one of the two groups R² or R⁴ is an amine and theother group is an aldehyde then 1B can be treated with an acid (such asp-toluenesulfonic acid) or a Lewis acid (such as tin tetrachloride) togive 1E, where X′ is —CR═N— or —N═CR—.

In Scheme 1, Step (ii), compounds of the structure 1A can be reactedwith 1C′ to form the linker X′ and give compounds of the structure 1C.The formation of the linker X′ in compounds with the structure 1C mayrequire a number of steps and the preparation of a number ofintermediates, and the use of protecting groups may also be required.

For example, if one of the two groups R² or R⁶ is a hydroxyl group andthe other group is a substituted alkylalcohol then 1A and 1C′ can betreated with a dehydrating agent (such as diisopropyl azodicarboxylate)in the presence of a phosphine, (such as triphenylphosphine) to give 1C,where X′ is an ether. Alternatively, if one of the two groups R² or R⁴is a hydroxyl and the other group is an alkyl group substituted with aleaving group (such as a halogen, or a mesylate) 1A and 1C′ can betreated with a base (such as diisopropylethylamine, potassium carbonateor sodium hydride) to form 1C, where X′ is an ether.

Alternatively, in Scheme 1, Step (ii), if one of the two groups R² or R⁶is a hydroxyl, or alkylalcohol and the other group is a carboxylic acid,then the carboxylic acid can be converted to an acyl halide (for exampleby treatment with thionyl chloride or oxalyl chloride), or to a mixedanhydride (for example by treatment with 2,4,6-trichlorobenzoyl chloridein the presence of a base such as diisopropylethylamine) or to anactivated ester (for example by treatment with HATU in the presence of abase such as diisopropylethylamine or pyridine, or treatment withdiisopropylcarbodiimide in the presence of HOBT), then 1A and 1C′ can becombined to form 1C, where X′ is an ester.

Alternatively, if one of the two groups R² or R⁶ is an amine, oralkylamine and the other group is a carboxylic acid, then the carboxylicacid can be converted to an acyl halide (for example by treatment withthionyl chloride or oxalyl chloride), or to a mixed anhydride (forexample by treatment with 2,4,6-trichlorobenzoyl chloride in thepresence of a base such as diisopropylethylamine), or to an activatedester (for example by treatment with HATU in the presence ofdisopropylethylamine or pyridine, or treatment withdiisopropylcarbodiimide in the presence of HOBT), then 1A and 1C′ can becombined to form 1C, where X′ is an amide.

Alternatively, if one of the two groups R² or R⁶ is an amine, orsubstituted alkylamine and the other group is an alkyl group substitutedwith a leaving group (such as a halogen, or a triflate) then 1A and 1C′can be treated with a base (such as diisopropylethylamine, pyridine orpotassium carbonate) to form 1C, where X′ is a substituted amine.

Alternatively, if one of the two groups R² or R⁶ is an aldehyde, and theother group is a phosphorane (such as an alkyltriphenylphosphorane) oran alkylphosphonate (such as an alkylphosphonic acid diethyl ester) then1A and 1C′ can be treated with a base (such as diisopropylethylamine orpotassium carbonate or sodium hexamethyldisilazide) to form 1C, where X′is an alkene which may, or may not be further substituted.

In Scheme 1, Step (v), compounds of structure 1E may be prepared fromcompounds of structure 1C by reaction of the groups R¹ and R⁵ under arange of conditions to form a carbon-carbon bond. If one of the groupsR¹ or R⁵ is a suitable group (such as a halide or triflate), and theother group is a borane, boronate or boronic acid then, in the presenceof a palladium catalyst (such as palladium chloride dppf), and in thepresence of a base (such as cesium carbonate), in an appropriate solvent(such as dioxane, water or tetrahydrofuran or mixtures thereof) andunder appropriate conditions (such as heating, for example heating at80-120° C. for 1-2 hours or microwave irradiation at 120-160° C. for 10minutes to 1 hour), 1C can be converted into 1E. A wide range ofappropriate reagents and conditions are known to those skilled in theart to couple organoboranes, boronates and boronic acids to givecompounds of the type 1E.

Alternatively, if one of the groups R¹ or R⁵ is a suitable group (suchas a halide or triflate), and the other group is a trialkylstannane, thecarbon-carbon bond can be formed in the presence of a palladium catalyst(such as palladium chloride dppf), in an appropriate solvent (such asdimethoxyethane or tetrahydrofuran) and under appropriate conditions(such as heating, at 80-120° C. for 1-2 hours or by microwaveirradiation at 120-160° C. for 10 minutes to 1 hour) to afford 1E. Awide range of appropriate reagents and conditions are known to thoseskilled in the art to couple aryl or heteroaryl stannanes to aryl orheteroaryl halides.

In Scheme 1, Step (iii), compounds of structure 1A may be reacted undera range of conditions with intermediates of the type 1D′ to givecompounds of structure 1D where D′ is a six- or seven-membered fusedheterocyclic ring and R⁹ and R¹⁰ are suitable functional groups that maybe used to form the B′-ring. The groups R¹ and R⁷ may be reactedtogether to form a carbon-carbon bond, and the groups R² and R⁸ may bereacted together to form the group X′. Methods to form bicycliccompounds of structure 1D from substituted phenyl rings of structure 1Aare well known to those skilled in the art (see ComprehensiveHeterocyclic Chemistry Ed.: Katritzky, Ramsden, Scriven, and Taylor,Elsevier, 2008).

For example, a compound of structure 1A, where R² is a hydroxyl groupand R¹ is hydrogen, can be treated with a suitably protected andsubstituted 3-halo-propanoic acid or ester in an appropriate solvent(such as tetrahydrofuran or dimethylformamide) and in the presence of abase (such as sodium carbonate or diisopropylethylamine) at atemperature between room temperature and the reflux temperature of thesolvent to give a compound of the type 1A, where R² is a substitutedoxypropanoic acid or ester. This intermediate may be treated with asuitable reagent (such as a strong acid, for example triflic acid) togive 1D where R⁹ is oxo, R¹⁰ is hydrogen and X′ is —OCH₂—.

Alternatively, a compound of structure 1A, where R² is a hydroxyl and R¹is hydrogen, can be treated with a propargyl halide or tosylate in thepresence of a base (such as potassium carbonate or cesium carbonate) ina solvent (such as acetone) at a temperature between room temperatureand the reflux temperature of the solvent to give a compound of type 1Ain which R² is a propargyloxyl group. This intermediate may be heated to˜200° C. or treated with an appropriate catalyst (such as a goldcatalyst, for example triphenylphosphine gold triflamide) in anappropriate solvent (such as toluene) at a temperature between 80° C.and the reflux temperature of the solvent to give a compound ofstructure 1D wherein X′ is —OCH₂—, R⁹ and R¹⁰ are H and the bond betweenis a double bond (i.e. a chromene).

Further modification of the intermediates of structure 1D having adouble bond between the carbons that R⁹ and R¹⁰ are attached to (such asa chromene) may be achieved, for example, by treatment with ahydroborating agent (such as borane-THF complex) followed by oxidationwith, for example, hydrogen peroxide to give a mixture of compounds ofstructure 1D wherein X′ is OCH₂, R⁹ is H and R¹⁰ is a hydroxyl group andwherein X′ is —OCH₂—, R⁹ is a hydroxyl and R¹⁰ is H which may beseparated by chromatography.

Further modification of an intermediate of structure 1D in which one ofR⁹ and R¹⁰ is H and the other is a hydroxyl may be carried out. Forexample, the intermediate may be oxidized by treatment with an oxidizingagent (such as Dess Martin periodinane) to give a compound of structure1D in which one of R⁹ and R¹⁰ is H the other is oxo.

Alternatively, a compound of structure 1A in which R¹ is an appropriategroup (such as a halogen, for example bromine or iodine, or a triflate)and R² is a protected amine (such as an acetamide or atrifluoroacetamide) may be coupled with a terminal alkyne in thepresence of a palladium catalyst (such as tetrakis(triphenylphosphine)palladium (0)) optionally in the presence of an additional coppercatalyst (such as copper (I) iodide) in the presence of a base or salt(such as triethylamine or potassium acetate), in a solvent (such astetrahydrofuran or dimethylformamide) at a temperature between roomtemperature and the reflux temperature of the solvent or by irradiationin the microwave at a temperature between 100° C. and 160° C. to give acompound of structure 1A in which R¹ is a substituted alkyne and R² is aprotected amine (such as an acetamide or a trifluoroacetamide).Alternatively, a compound of structure 1A in which R¹ is an appropriategroup (such as a halogen, for example bromine or iodine, or a triflate)and R² is a protected amine (such as an acetamide or atrifluoroacetamide) may be coupled with an acetylenic stannane in thepresence of a palladium catalyst (such as palladium chloride dppf) in anappropriate solvent (such as dioxane, dimethoxyethane ortetrahydrofuran) at a temperature between room temperature and thereflux temperature of the solvent or alternatively by irradiation in themicrowave at a temperature between 100° C. and 160° C. to give acompound of structure 1A in which R¹ is an alkyne and R² is a protectedamine (such as an acetamide or a trifluoroacetamide).

In Scheme 1, Step (iii), a compound of structure 1A in which R¹ is anappropriately substituted alkyne and R² is a protected amine (such as anacetamide of a trifluoroacetamide) may be treated with a base (such aspotassium carbonate or sodium methoxide) in an appropriate solvent (suchas acetone, DMF or methanol) at a temperature between room temperatureand the reflux temperature of the solvent to give a compound ofstructure 1D in which X′ is NH. Alternatively, a compound of structure1A in which R¹ is an appropriately substituted alkyne and R² is aprotected amine (such as an acetamide of a trifluoroacetamide) may betreated with a palladium catalyst (such asbis-(triphenylphosphine)palladium chloride) in the presence of a base(such as triethylamine) and an appropriate catalyst (such as copper(I)iodide) in a solvent (such as dimethylformamide) at a temperaturebetween room temperature and the reflux temperature of the solvent togive a compound of structure 1D in which X′ is NH.

The general synthetic strategy to elaborate 1D is shown in Scheme 2.

In Scheme 2, compounds of structure TD may be converted to a variety ofcompounds of structure 1E using reactions known to those skilled in theart. In some cases modifications to the groups R⁹ and R¹⁰ in 1D may berequired in order to be able to generate the require ring systems. Oneskilled in the art will recognize that it may be necessary for variousfunctional groups to be protected prior to reaction. Specific steps inthe synthetic procedures are described in more detail below.

In Scheme 2, Step (i), 1D in which R⁹ and R¹⁰ are both H and the bondbetween the carbon atoms is a double bond, may be treated with diethylzinc and di-iodomethane optionally in the presence of additionalreagents (such as trifluoroacetic acid or zinc iodide) in a solvent(such as 1,2-dichloroethane) at a temperature between −78° C. and roomtemperature to give compounds of structure 2A in which the B′ ring is acyclopropyl ring. Alternatively, compounds of structure 1D in which R⁹and R¹⁰ are both H and the bond between the carbon atoms is a doublebond, may be treated with trimethyl sulfoxonium iodide or trimethylsulphonium iodide in the presence of a base (such as sodium hydride) ina solvent (such as dimethyl sulfoxide) at a temperature between roomtemperature and 100° C. Alternatively, compounds of structure 1D inwhich R⁹ and R¹⁰ are both H and the bond between the carbon atoms is adouble bond, may be treated with diazomethane in the presence of acatalyst (such as palladium acetate) in a solvent such as diethyl etherat a temperature between 0° C. and room temperature.

Alternatively, compounds of structure 2A may be prepared in a two stepprocedure. For example, in Scheme 2, Step (ii), 1D in which R⁹ and R¹⁰are both H and the bond between the carbon atoms is a double bond, maybe treated with trimethylsilyl diazomethane in the presence of acatalyst (such as palladium acetate) in a solvent (such as diethylether) at a temperature between 0° C. and room temperature to give theintermediate 2A′ in which J is H and J′ is a trimethyl silyl group. InScheme 2, Step (iii), intermediates 2A′ in which J is H and J′ is atrimethyl silyl group may be converted to compounds of structure 2A bytreatment with a source of fluoride, (for example tetrabutyl ammoniumfluoride) in a solvent (such as tetrahydrofuran) at a temperaturebetween 0° C. and room temperature.

Alternatively in Scheme 2, Step (ii), 1D in which R⁹ and R¹⁰ are both Hand the bond between the carbon atoms is a double bond, may be treatedwith a haloform (such as chloroform or bromoform) in the presence of abase such as sodium hydroxide or potassium t-butoxide in the presence ofa catalyst (such as triethylbenzylammonium chloride or tetrabutylammonium bromide) in a mixture of water and a halogenated solvent (suchas dichloromethane or dichloroethane) or alternatively in excess of thehaloform at a temperature between room temperature and 80° C. to givethe intermediate 2A′ in which J and J′ are both chlorine or bromine. InScheme 2, Step (iii), the intermediates 2A′ in which J and J′ are bothchlorine or bromine may be converted to compounds of structure 2A bytreatment with a base (such as sodium methoxide or sodium t-butoxide) ina solvent (such as tetrahydrofuran) at a temperature between roomtemperature and the reflux temperature of the solvent. Alternatively,the intermediates 2A′ in which J and J′ are both chlorine or bromine maybe converted to compounds of structure 2A by reduction; for example, bytreatment with lithium aluminium hydride in a solvent (such astetrahydrofuran) at a temperature between 0° C. and the refluxtemperature of the solvent or alternatively, for example byhydrogenation using a catalyst (such as palladium on carbon) in asolvent (such as methanol or ethanol), optionally in the presence of abase (such as triethylamine). Alternatively, the intermediates 2A′ inwhich J and J′ are both chlorine or bromine may be converted tocompounds of structure 2A under radical conditions; for example, bytreatment with a tin hydride (such as tributyl tin hydride) optionallyin the presence of a radical initiator (such asazo-bis-isobutyronitrile) in a solvent (such as toluene) at atemperature between room temperature and the reflux temperature of thesolvent.

In Scheme 2, Step (iv), 1D in which X′ includes a carbonyl (for examplewhere X′ is —O—C(O)—) and R⁹ and R¹⁰ are both H and the bond between thecarbon atoms is a double bond, may be converted to the correspondingcompounds 2B by treatment with ethylene in a solvent (such asdichloromethane) under photochemical conditions.

Alternatively compounds of structure 2B may be prepared in a multi-stepprocedure. For example, in Scheme 2, Step (v), 1D in which both R⁹ andR¹⁰ are both H and the bond between the two carbon atoms is a doublebond may be treated with an acrylate (such as ethyl acrylate) in asolvent (such as acetonitrile) under photochemical conditions to give anintermediate 2B′ in which J″ is an ester group (such as an ethyl ester).The ester may be hydrolysed by, for example, treatment with sodiumhydroxide or lithium hydroxide in a solvent such as aqueous ethanol oraqueous dioxane at a temperature between room temperature and the refluxtemperature of the solvent to give an intermediate of structure 2B′ inwhich J″ is a carboxylic acid. In Scheme 2, Step (vi), the acid may beremoved for example by heating in, for example, quinoline optionally inthe presence of a catalyst (such as copper) to around 200° C.

In Scheme 2, Step (vii), 1D in which R¹⁰ is a hydroxyl and R⁹ is a groupCH₂OH may be treated with a sulfonyl chloride (such as 4-toluenesulfonylchloride or methanesulfonyl chloride) in the presence of a base (such astriethylamine), optionally in the presence of 4-dimethylaminopyridine,in a solvent (such as dichloromethane or toluene) at a temperaturebetween room temperature and the reflux temperature of the solvent. Theproduct may be treated with a base (such as triethylamine,diisopropylethylamine or sodium hydride) in an appropriate solvent (suchas dichloromethane, tetrahydrofuran or DMF) to give a compound ofstructure 2C.

In Scheme 2, Step (viii), 1D in which R⁹ is CH₂CH₂OH and R¹⁰ is CH₂OHmay be converted to compounds 2D. One of the hydroxyl groups may need tobe protected and the other is treated with a sulfonyl chloride (such as4-toluenesulfonyl chloride or methanesulfonyl chloride) in the presenceof a base (such as triethylamine) optionally in the presence of4-dimethylaminopyridine, in a solvent (such as dichloromethane ortoluene) at a temperature between room temperature and the refluxtemperature of the solvent. After deprotection of the remaining hydroxylgroup, the intermediate may be treated with a base (such astriethylamine, diisopropylethylamine or sodium hydride) in a solvent(such as dichloromethane, tetrahydrofuran or dimethylformamide at atemperature between room temperature and the reflux temperature of thesolvent to give a compound of structure 2D.

Alternatively, compounds of structure 2D may be prepared in a 2 stepprocedure. For example, in Scheme 2, Step (ix), 1D in which R⁹ isCH₂CO₂H and R¹⁰ is CH₂OH may be converted to compounds of structure 2D′.The carboxylic acid may be converted to an acid chloride (by treatmentwith, for example, thionyl chloride or oxalyl chloride, optionally inthe presence of a catalytic amount of DMF in a solvent such asdichloromethane or toluene) or to a mixed anhydride (for example bytreatment with 2,4,6-trichlorobenzoyl chloride in the presence of a basesuch as diisopropylethylamine) or to an activated ester (for example bytreatment with HATU in the presence of a base such asdiisopropylethylamine or pyridine, or treatment withdiisopropylcarbodiimide in the presence of HOBT). The acid chloride,mixed anhydride or activated ester may then be treated with a base (suchas triethylamine or pyridine), in a solvent (such dichloromethane ortoluene) to give the compound of structure 2D′. In Scheme 2, Step (x),compounds of structure 2D′ may be converted to compounds of structure 2Dby reduction, for example, by treatment with lithium aluminium hydride,sodium diisobutylaluminium hydride or borane-dimethyl sulfide complex,in an appropriate solvent (such as tetrahydrofuran) at a temperaturebetween −78° C. and room temperature.

In Scheme 2, Step (xi), 1D in which R⁹ is CH₂CH₂OH and R¹⁰ is a hydroxylmay be treated with a sulfonyl chloride (such as 4-toluenesulfonylchloride or methanesulfonyl chloride) in the presence of a base (such astriethylamine), optionally in the presence of 4-dimethylaminopyridine,in a solvent (such as dichloromethane or toluene) at a temperaturebetween room temperature and the reflux temperature of the solvent,followed by treatment with a base (such as triethylamine,diisopropylethylamine or sodium hydride) in an appropriate solvent (suchas dichloromethane, tetrahydrofuran or DMF) at a temperature betweenroom temperature and the reflux temperature of the solvent to give acompound of structure 2E.

Alternatively, compounds of structure 2E may be prepared in a 2 stepprocedure. In Scheme 2, Step (xii), 1D in which R⁹ is H and R¹⁰ is oxomay be converted to compounds of structure 2E′ by treatment withchloroacetaldehyde or bromoacetaldehyde in the presence of an aqueousbase (such as sodium bicarbonate or sodium hydroxide in water) at atemperature between 0° C. and room temperature, followed by treatmentwith an acid (such as concentrated sulfuric acid) in a mixture of waterand an organic solvent (such as ethyl acetate).

In Scheme 2, Step (xiii), compounds of structure 2E may be prepared fromcompounds of structure 2E′ by hydrogenation in the presence of a metalcatalyst (such as palladium or palladium hydroxide on a solid supportsuch as carbon) in a solvent (such as an ether, for exampletetrahydrofuran or dioxane, or an alcohol, such as methanol or ethanol),optionally in the presence of an acid (such as acetic acid). Dependingupon the nature of the linker X′, the bond between the two rings may bereduced or not to give either a tetrahydrofuran or a dihydrofuran. Forexample, if X′ is —N═C— then the B′ ring in 2E will be a dihydrofuranwhereas if X′ is —OCH₂— then the B′ ring will be a tetrahydrofuran.

In Scheme 1, Step (vii), compounds of general structure 1E may beconverted to compounds of General Formula I by the conversion of thegroup G′ to a carboxylic acid. If the group G′ is a carboxylic ester(such as a methyl, tert-butyl or benzyl ester) then a variety ofreagents and conditions can be used to convert 1E into a compound of theGeneral Formula I. For example, if G′ is a methyl, ethyl or benzylester, it may be converted to a carboxylic acid by treatment with aninorganic base (such as lithium hydroxide or sodium hydroxide) in asolvent (such as methanol, dioxane or water, or mixtures thereof) at atemperature between room temperature and the reflux temperature of thesolvent, or alternatively by microwave irradiation at 120-180° C. for 10minutes to 1 hour. Alternatively if G′ is a benzyl ester it may beconverted to a carboxylic acid by hydrogenation in the presence of acatalyst (such as palladium on a solid support such as carbon) in asolvent (such as dioxane or ethyl acetate). Alternatively if G′ is atert-butyl ester, it may be converted to a carboxylic acid by treatmentwith an acid (such as trifluoromethanesulfonic acid or hydrogenchloride) in a solvent (such as dichloromethane or dioxane).

Alternatively, if the group G′ is a nitrile, it may be converted into acarboxylic acid by treatment with aqueous acid (such as a mineral acid,for example hydrochloric acid) under appropriate conditions (such asheating, for example to reflux); or by treatment with aqueous base (suchas an aqueous hydroxide, for example aqueous sodium hydroxide) underappropriate conditions (such as heating, for example to reflux).

Alternatively, if the group G′ is an aldehyde (CHO) or a hydroxymethyl(CH₂OH) moiety then it may be converted into a carboxylic acid bytreatment with a suitable oxidising reagent (such as potassiumpermanganate or chromic acid).

The general synthetic strategy to modify the group G is depicted inScheme 3. The G group may be introduced and/or modified either before,during or after the assembly of the tricyclic ring system. Specificsteps used to assemble sulfonamide are described in more detail below.

In Scheme 3, the asterisks denote either the presence of the groups R¹and R² (as shown in Scheme 1) or the presence of the D′ and B′ rings, orintermediates towards the preparation of the rings (as shown in Schemes1 and 2).

In Scheme 3, Step (i), compounds of structure 3A in which G is a nitrogroup may be converted to compounds 3B by reduction, for example bycatalytic hydrogenation in the presence of a metal catalyst (such aspalladium on a solid support such as carbon) in a solvent (such as anether, for example tetrahydrofuran, or an alcohol, for example methanolor ethanol). Alternatively, compounds of structure 3A in which G is anitro group may be converted to compounds of structure 3B by chemicalreduction. For example, the reduction may be achieved using a metal ormetal salt (such as iron, zinc or tin (II) chloride) in the presence ofan acid (such as hydrochloric acid or acetic acid).

In Scheme 3, Step (i), compounds of structure 3A in which G is aprotected amino group may be converted to compounds of structure 3B byremoval of the protecting groups. Protecting groups for amino groups arewell known to those skilled in the art and methods for their removal areequally well known [for example, see Greene, Wuts, Protective Groups inOrganic Synthesis. 2nd Ed. (1999)]. For example, compounds of structure3A in which F is an amino group protected with one or two Boc groups maybe converted to compounds of structure 3B by treatment with an acid(such as trifluoroacetic acid, formic acid or hydrogen chloride) in asolvent (such as dichloromethane or dioxane).

Alternatively, in Scheme 3, Step (i), compounds of structure 3A in whichG is a pivaloyl protected aniline may be converted to compounds ofstructure 3B by treatment with an acid (such as concentrated sulfuricacid) in a solvent (such as methanol) at a temperature between roomtemperature and the reflux temperature of the solvent.

In Scheme 3, Step (ii), compounds of structure 3B may be converted tocompounds of structure 3C by treatment with an appropriate sulfonylchloride (such as a substituted or unsubstituted benzene sulfonylchloride) or an activated sulfonate ester (such as a pentafluorophenylsulfonate ester) in the presence of a suitable base (such as pyridine,diisopropylethylamine or cesium carbonate) in a suitable solvent (suchas dichloromethane or dimethylformamide) at a temperature between roomtemperature and the reflux temperature of the solvent.

Intermediates towards the preparation of compounds of Formula 1 or, forexample, General Formula 1 may require reduction of an aromatic ringsystem to give the saturated ring system required in the compounds ofFormula 1. This hydrogenation may be carried out by hydrogenation of theintermediates in the presence of a metal catalyst (for example palladiumor palladium hydroxide on a solid support, such as carbon) in a solvent(such as ethanol, ethyl acetate or dioxane) optionally in the presenceof an acid (such as acetic acid). The reduction of the aromatic ringsmay be carried out before the formation of the tricyclic ring system orafter it or at any stage during the synthesis as will be recognized bythose skilled in the art.

Compounds of any of Formula I, Formula II or, for example, GeneralFormula I as depicted above, or any of the intermediates described inthe schemes above, can be further derivatised by using one or morestandard synthetic methods known to those skilled in the art. Suchmethods can involve substitution, oxidation or reduction reactions.These methods can also be used to obtain or modify compounds of GeneralFormula I or any preceding intermediates by modifying, introducing orremoving appropriate functional groups. Particular substitutionapproaches include alkylation, arylation, heteroarylation, acylation,thioacylation, halogenation, sulfonylation, nitration, formylation,hydrolysis and coupling procedures. These procedures can be used tointroduce a functional group onto the parent molecule (such as thenitration or sulfonylation of aromatic rings) or to couple two moleculestogether (for example to couple an amine to a carboxylic acid to affordan amide; or to form a carbon-carbon bond between two heterocycles). Forexample, alcohol or phenol groups can be converted to ether groups bycoupling a phenol with an alcohol in a solvent (such as tetrahydrofuran)in the presence of a phosphine (such as triphenylphosphine) and adehydrating agent (such as diethyl, diisopropyl or dimethylazodicarboxylate). Alternatively, ether groups can be prepared bydeprotonation of an alcohol, using a suitable base (such as sodiumhydride) followed by the addition of an alkylating agent (such as analkyl halide or an alkyl sulfonate).

In another example, a primary or secondary amine can be alkylated usinga reductive alkylation procedure. For example, the amine can be treatedwith an aldehyde and a borohydride (such as sodiumtriacetoxyborohydride, or sodium cyanoborohydride in a solvent (such asa halogenated hydrocarbon, for example dichloromethane, or an alcohol,for example ethanol) and, where necessary, in the presence of an acid(such as acetic acid).

In another example, hydroxy groups (including phenolic OH groups) can beconverted into leaving groups, such as halogen atoms or sulfonyloxygroups (such as alkylsulfonyloxy, for exampletrifluoromethanesulfonyloxy, or aryl suphonyloxy, for examplep-toluenesulfonyloxy) using conditions known to those skilled in theart. For example, an aliphatic alcohol can be reacted with thionylchloride in a halogenated hydrocarbon (such as dichloromethane) toafford the corresponding alkyl chloride. A base (such as triethylamine)can also be used in the reaction.

In another example, ester groups can be converted to the correspondingcarboxylic acid by acid- or base-catalysed hydrolysis depending on thenature of the ester group. Acid catalysed hydrolysis can be achieved bytreatment with an organic or inorganic acid (such as trifluoroaceticacid in an aqueous solvent, or a mineral acid such as hydrochloric acidin a solvent such as dioxane). Base catalysed hydrolysis can be achievedby treatment with an alkali metal hydroxide (such as lithium hydroxidein an aqueous alcohol, for example methanol).

In another example, aromatic halogen substituents in the compounds maybe subjected to halogen-metal exchange by treatment with a base (such asa lithium base, for example n-butyl or t-butyl lithium) optionally at alow temperature (such as −78° C.) in a solvent (such as tetrahydrofuran)and the mixture may then be quenched with an electrophile to introduce adesired substituent. Thus, for example, a formyl group can be introducedby using dimethylformamide as the electrophile. Aromatic halogensubstituents can also be subjected to palladium catalysed reactions tointroduce groups such as carboxylic acids, esters, cyano or aminosubstituents.

In another example, an aryl, or heteroaryl ring substituted with anappropriate leaving group (such as a halogen or sulfonyl ester, forexample a triflate) can undergo a palladium catalysed coupling reactionwith a wide variety of substrates to form a carbon-carbon bond. Forexample, a Heck reaction can be used to couple such a ring system to analkene (which may, or may not, be further substituted) by treatment withan organopalladium complex (such astetrakis(triphenylphosphine)palladium(0), palladium (II) acetate orpalladium (II) chloride) in the presence of a ligand (such as aphosphine, for example triphenylphosphine) in the presence of a base(such as potassium carbonate or a tertiary amine, for example,triethylamine), in an appropriate solvent (such as tetrahydrofuran orDMF), under appropriate conditions (such as heating to, for example,50-120° C.). In another example, a Sonogashira reaction can be used tocouple such a ring system to an alkyne (which may, or may not be furthersubstituted) by treatment with a palladium complex (such astetrakis(triphenylphosphine)palladium(0)) and a halide salt of copper(I) (such as copper (I) iodide), in the presence of a base (such as apotassium carbonate or a tertiary amine, for example, triethylamine), inan appropriate solvent (such as tetrahydrofuran or dimethylformamide),under appropriate conditions (such as heating to, for example, 50-120°C.). In another example, a Stille reaction can be used to couple such aring system to an alkene, by treatment with an organotin compound (suchas an alkynyltin or alkenyltin reagent, for example analkenyltributylstannane) in the presence of a palladium complex (such astetrakis(triphenylphosphine)palladium(0)), with, or without the presenceof a salt (such as a copper (I) halide), in an appropriate solvent (suchas dioxane or dimethylformamide), under appropriate conditions (such asheating to, for example, 50-120° C.).

Particular oxidation approaches include dehydrogenations andaromatisation, decarboxylation and the addition of oxygen to certainfunctional groups. For example, aldehyde groups can be prepared byoxidation of the corresponding alcohol using conditions well known tothose skilled in the art. For example, an alcohol can be treated with anoxidising agent (such as Dess-Martin periodinane) in a solvent (such asa halogenated hydrocarbon, for example dichloromethane). Alternativeoxidising conditions can be used, such as treatment with oxalyl chlorideand an activating amount of dimethylsulfoxide and subsequent quenchingby the addition of an amine (such as triethylamine). Such a reaction canbe carried out in an appropriate solvent (such as a halogenatedhydrocarbon, for example dichloromethane) and under appropriateconditions (such as cooling below room temperature, for example to −78°C. followed by warming to room temperature). In another example, sulfuratoms can be oxidised to the corresponding sulfoxide or sulfone using anoxidising agent (such as a peroxy acid, for example3-chloroperoxybenzoic acid) in an inert solvent (such as a halogenatedhydrocarbon, for example dichloromethane) at around ambient temperature.

Particular reduction approaches include the removal of oxygen atoms fromparticular functional groups or saturation (or partial saturation) ofunsaturated compounds including aromatic or heteroaromatic rings. Forexample, primary alcohols can be generated from the corresponding esteror aldehyde by reduction, using a metal hydride (such as lithiumaluminium hydride or sodium borohydride in a solvent such as methanol).Alternatively, CH₂OH groups can be generated from the correspondingcarboxylic acid by reduction, using a metal hydride (such as lithiumaluminium hydride in a solvent such as tetrahydrofuran). In anotherexample, a nitro group may be reduced to an amine by catalytichydrogenation in the presence of a metal catalyst (such as palladium ona solid support such as carbon) in a solvent (such as an ether, forexample tetrahydrofuran, or an alcohol, such as methanol), or bychemical reduction using a metal (such as zinc, tin or iron) in thepresence of an acid (such as acetic acid or hydrochloric acid). In afurther example an amine can be obtained by reduction of a nitrile, forexample by catalytic hydrogenation in the presence of a metal catalyst(such as palladium on a solid support such as carbon), or Raney nickelin a solvent (such as tetrahydrofuran) and under suitable conditions(such as cooling to below room temperature, for example to −78° C., orheating, for example to reflux).

Salts of compounds of General Formula I can be prepared by the reactionof a compound of General Formula I with an appropriate acid or base in asuitable solvent, or mixture of solvents (such as an ether, for example,diethyl ether, or an alcohol, for example ethanol, or an aqueoussolvent) using conventional procedures. Salts of compound of GeneralFormula I can be exchanged for other salts by treatment usingconventional ion-exchange chromatography procedures.

Where it is desired to obtain a particular enantiomer of a compound ofGeneral Formula I, this may be produced from a corresponding mixture ofenantiomers by employing any suitable conventional procedure forresolving enantiomers. For example, diastereomeric derivatives (such assalts) can be produced by reaction of a mixture of enantiomers of acompound of General Formula I (such a racemate) and an appropriatechiral compound (such as a chiral base). The diastereomers can then beseparated by any conventional means such as crystallisation, and thedesired enantiomer recovered (such as by treatment with an acid in theinstance where the diastereomer is a salt). Alternatively, a racemicmixture of esters can be resolved by kinetic hydrolysis using a varietyof biocatalysts (for example, see Patel Stereoselective Biocatalysts,Marcel Decker; New York 2000).

In another resolution process a racemate of compounds of General FormulaI can be separated using chiral High Performance Liquid Chromatography.Alternatively, a particular enantiomer can be obtained by using anappropriate chiral intermediate in one of the processes described above.Chromatography, recrystallisation and other conventional separationprocedures may also be used with intermediates or final products whereit is desired to obtain a particular geometric isomer of the invention.

II. Methods

Another aspect of the invention provides methods of modulating theactivity of MetAP2. Such methods comprise exposing said receptor to acompound described herein. In some embodiments, the compound utilized byone or more of the foregoing methods is one of the generic, subgeneric,or specific compounds described herein, such as a compound of Formula I,Ia, Ib, Ic, Id, Ie, If, II, III or IV. The ability of compoundsdescribed herein to modulate or inhibit MetAP2 can be evaluated byprocedures known in the art and/or described herein. Another aspect ofthe invention provides methods of treating a disease associated withexpression or activity of MetAP2 in a patient. For example, acontemplated method includes administering a disclosed compound in anamount sufficient to establish inhibition of intracellular MetAP2effective to increase thioredoxin production in the patient and toinduce multi organ stimulation of anti-obesity processes in the subject,for example, by administering a disclosed compound in an amountinsufficient to reduce angiogenesis in the patient.

In certain embodiments, the invention provides a method of treating andor ameliorating obesity in a patient by administering an effectiveamount of a disclosed compound. Also provided herein are methods forinducing weight loss in a patient in need thereof. Contemplated patientsinclude not only humans, but other animals such as companion animals(e.g., dogs, cats).

Other contemplated methods of treatment include method of treating orameliorating an obesity-related condition or co-morbidity, byadministering a compound disclosed herein to a subject. For example,contemplated herein are methods for treating type 2 diabetes in apatient in need thereof.

Exemplary co-morbidities include cardiac disorders, endocrine disorders,respiratory disorders, hepatic disorders, skeletal disorders,psychiatric disorders, metabolic disorders, and reproductive disorders.

Exemplary cardiac disorders include hypertension, dyslipidemia, ischemicheart disease, cardiomyopathy, cardiac infarction, stroke, venousthromboembolic disease and pulmonary hypertension. Exemplary endocrinedisorders include type 2 diabetes and latent autoimmune diabetes inadults. Exemplary respiratory disorders include obesity-hypoventilationsyndrome, asthma, and obstructive sleep apnea. An exemplary hepaticdisorder is nonalcoholic fatty liver disease. Exemplary skeletaldisorders include back pain and osteoarthritis of weight-bearing joints.Exemplary metabolic disorders include Prader-Willi Syndrome andpolycystic ovary syndrome. Exemplary reproductive disorders includesexual dysfunction, erectile dysfunction, infertility, obstetriccomplications, and fetal abnormalities. Exemplary psychiatric disordersinclude weight-associated depression and anxiety.

In particular, in certain embodiments, the invention provides a methodof treating the above medical indications comprising administering to asubject in need thereof a therapeutically effective amount of a compounddescribed herein, such as a compound of Formula I, Ia, Ib, Ic, Id, Ie,If, II, III or IV.

Obesity or reference to “overweight” refers to an excess of fat inproportion to lean body mass. Excess fat accumulation is associated withincrease in size (hypertrophy) as well as number (hyperplasia) ofadipose tissue cells. Obesity is variously measured in terms of absoluteweight, weight:height ratio, distribution of subcutaneous fat, andsocietal and esthetic norms. A common measure of body fat is Body MassIndex (BMI). The BMI refers to the ratio of body weight (expressed inkilograms) to the square of height (expressed in meters). Body massindex may be accurately calculated using either of the formulas: weight(kg)/height² (m²) (SI) or 703×weight (lb)/height² (in²) (US).

In accordance with the U.S. Centers for Disease Control and Prevention(CDC), an overweight adult has a BMI of 25 kg/m² to 29.9 kg/m², and anobese adult has a BMI of 30 kg/m² or greater. A BMI of 40 kg/m² orgreater is indicative of morbid obesity or extreme obesity. Obesity canalso refer to patients with a waist circumference of about 102 cm formales and about 88 cm for females. For children, the definitions ofoverweight and obese take into account age and gender effects on bodyfat. Patients with differing genetic background may be considered“obese” at a level differing from the general guidelines, above.

The compounds of the present invention also are useful for reducing therisk of secondary outcomes of obesity, such as reducing the risk of leftventricular hypertrophy. Methods for treating patients at risk ofobesity, such as those patients who are overweight, but not obese, e.g.with a BMI of between about 25 and 30 kg/m², are also contemplated. Incertain embodiments, a patient is a human.

BMI does not account for the fact that excess adipose can occurselectively in different parts of the body, and development of adiposetissue can be more dangerous to health in some parts of the body ratherthan in other parts of the body. For example, “central obesity”,typically associated with an “apple-shaped” body, results from excessadiposity especially in the abdominal region, including belly fat andvisceral fat, and carries higher risk of co-morbidity than “peripheralobesity”, which is typically associated with a “pear-shaped” bodyresulting from excess adiposity especially on the hips. Measurement ofwaist/hip circumference ratio (WHR) can be used as an indicator ofcentral obesity. A minimum WHR indicative of central obesity has beenvariously set, and a centrally obese adult typically has a WHR of about0.85 or greater if female and about 0.9 or greater if male.

Methods of determining whether a subject is overweight or obese thataccount for the ratio of excess adipose tissue to lean body mass involveobtaining a body composition of the subject. Body composition can beobtained by measuring the thickness of subcutaneous fat in multipleplaces on the body, such as the abdominal area, the subscapular region,arms, buttocks and thighs. These measurements are then used to estimatetotal body fat with a margin of error of approximately four percentagepoints. Another method is bioelectrical impedance analysis (BIA), whichuses the resistance of electrical flow through the body to estimate bodyfat. Another method is using a large tank of water to measure bodybuoyancy. Increased body fat will result in greater buoyancy, whilegreater muscle mass will result in a tendency to sink.

In another aspect, the invention provides methods for treating anoverweight or obese subject involving determining a level of at leastone biomarker related to being overweight or obese in the subject, andadministering an effective amount of a disclosed compound to achieve atarget level in the subject. Exemplary biomarkers include body weight,Body Mass Index (BMI), Waist/Hip ratio WHR, plasma adipokines, and acombination of two or more thereof.

In certain embodiments, the compound utilized by one or more of theforegoing methods is one of the generic, subgeneric, or specificcompounds described herein, such as a compound of Formula I, Ia, Ib, Ic,Id, Ie, If, II, III or IV.

The compounds of the invention may be administered to patients (animalsand humans) in need of such treatment in dosages that will provideoptimal pharmaceutical efficacy. It will be appreciated that the doserequired for use in any particular application will vary from patient topatient, not only with the particular compound or composition selected,but also with the route of administration, the nature of the conditionbeing treated, the age and condition of the patient, concurrentmedication or special diets then being followed by the patient, andother factors which those skilled in the art will recognize, with theappropriate dosage ultimately being at the discretion of the attendantphysician. For treating clinical conditions and diseases noted above, acompound of this invention may be administered orally, subcutaneously,topically, parenterally, by inhalation spray or rectally in dosage unitformulations containing conventional non-toxic pharmaceuticallyacceptable carriers, adjuvants and vehicles. Parenteral administrationmay include subcutaneous injections, intravenous or intramuscularinjections or infusion techniques.

Treatment can be continued for as long or as short a period as desired.The compositions may be administered on a regimen of, for example, oneto four or more times per day. A suitable treatment period can be, forexample, at least about one week, at least about two weeks, at leastabout one month, at least about six months, at least about 1 year, orindefinitely. A treatment period can terminate when a desired result,for example a weight loss target, is achieved. A treatment regimen caninclude a corrective phase, during which dose sufficient to providereduction of weight is administered, and can be followed by amaintenance phase, during which a e.g. a lower dose sufficient toprevent weight gain is administered. A suitable maintenance dose islikely to be found in the lower parts of the dose ranges providedherein, but corrective and maintenance doses can readily be establishedfor individual subjects by those of skill in the art without undueexperimentation, based on the disclosure herein. Maintenance doses canbe employed to maintain body weight in subjects whose body weight hasbeen previously controlled by other means, including diet and exercise,bariatric procedures such as bypass or banding surgeries, or treatmentsemploying other pharmacological agents.

III. Pharmaceutical Compositions and Kits

Another aspect of the invention provides pharmaceutical compositionscomprising compounds as disclosed herein formulated together with apharmaceutically acceptable carrier. In particular, the presentdisclosure provides pharmaceutical compositions comprising compounds asdisclosed herein formulated together with one or more pharmaceuticallyacceptable carriers. These formulations include those suitable for oral,rectal, topical, buccal, parenteral (e.g., subcutaneous, intramuscular,intradermal, or intravenous) rectal, vaginal, or aerosol administration,although the most suitable form of administration in any given case willdepend on the degree and severity of the condition being treated and onthe nature of the particular compound being used. For example, disclosedcompositions may be formulated as a unit dose, and/or may be formulatedfor oral or subcutaneous administration.

Exemplary pharmaceutical compositions of this invention may be used inthe form of a pharmaceutical preparation, for example, in solid,semisolid or liquid form, which contains one or more of the compound ofthe invention, as an active ingredient, in admixture with an organic orinorganic carrier or excipient suitable for external, enteral orparenteral applications. The active ingredient may be compounded, forexample, with the usual non-toxic, pharmaceutically acceptable carriersfor tablets, pellets, capsules, suppositories, solutions, emulsions,suspensions, and any other form suitable for use. The active objectcompound is included in the pharmaceutical composition in an amountsufficient to produce the desired effect upon the process or conditionof the disease.

For preparing solid compositions such as tablets, the principal activeingredient may be mixed with a pharmaceutical carrier, e.g.,conventional tableting ingredients such as corn starch, lactose,sucrose, sorbitol, talc, stearic acid, magnesium stearate, dicalciumphosphate or gums, and other pharmaceutical diluents, e.g., water, toform a solid preformulation composition containing a homogeneous mixtureof a compound of the invention, or a non-toxic pharmaceuticallyacceptable salt thereof. When referring to these preformulationcompositions as homogeneous, it is meant that the active ingredient isdispersed evenly throughout the composition so that the composition maybe readily subdivided into equally effective unit dosage forms such astablets, pills and capsules.

In solid dosage forms for oral administration (capsules, tablets, pills,dragees, powders, granules and the like), the subject composition ismixed with one or more pharmaceutically acceptable carriers, such assodium citrate or dicalcium phosphate, and/or any of the following: (1)fillers or extenders, such as starches, lactose, sucrose, glucose,mannitol, and/or silicic acid; (2) binders, such as, for example,carboxymethylcellulose, alginates, gelatin, polyvinyl pyrrolidone,sucrose and/or acacia; (3) humectants, such as glycerol; (4)disintegrating agents, such as agar-agar, calcium carbonate, potato ortapioca starch, alginic acid, certain silicates, and sodium carbonate;(5) solution retarding agents, such as paraffin; (6) absorptionaccelerators, such as quaternary ammonium compounds; (7) wetting agents,such as, for example, acetyl alcohol and glycerol monostearate; (8)absorbents, such as kaolin and bentonite clay; (9) lubricants, such atalc, calcium stearate, magnesium stearate, solid polyethylene glycols,sodium lauryl sulfate, and mixtures thereof, and (10) coloring agents.In the case of capsules, tablets and pills, the compositions may alsocomprise buffering agents. Solid compositions of a similar type may alsobe employed as fillers in soft and hard-filled gelatin capsules usingsuch excipients as lactose or milk sugars, as well as high molecularweight polyethylene glycols and the like.

A tablet may be made by compression or molding, optionally with one ormore accessory ingredients. Compressed tablets may be prepared usingbinder (for example, gelatin or hydroxypropylmethyl cellulose),lubricant, inert diluent, preservative, disintegrant (for example,sodium starch glycolate or cross-linked sodium carboxymethyl cellulose),surface-active or dispersing agent. Molded tablets may be made bymolding in a suitable machine a mixture of the subject compositionmoistened with an inert liquid diluent. Tablets, and other solid dosageforms, such as dragees, capsules, pills and granules, may optionally bescored or prepared with coatings and shells, such as enteric coatingsand other coatings well known in the pharmaceutical-formulating art.

Compositions for inhalation or insufflation include solutions andsuspensions in pharmaceutically acceptable, aqueous or organic solvents,or mixtures thereof, and powders. Liquid dosage forms for oraladministration include pharmaceutically acceptable emulsions,microemulsions, solutions, suspensions, syrups and elixirs. In additionto the subject composition, the liquid dosage forms may contain inertdiluents commonly used in the art, such as, for example, water or othersolvents, solubilizing agents and emulsifiers, such as ethyl alcohol,isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol,benzyl benzoate, propylene glycol, 1,3-butylene glycol, oils (inparticular, cottonseed, groundnut, corn, germ, olive, castor and sesameoils), glycerol, tetrahydrofuryl alcohol, polyethylene glycols and fattyacid esters of sorbitan, cyclodextrins and mixtures thereof.

Suspensions, in addition to the subject composition, may containsuspending agents as, for example, ethoxylated isostearyl alcohols,polyoxyethylene sorbitol and sorbitan esters, microcrystallinecellulose, aluminum metahydroxide, bentonite, agar-agar and tragacanth,and mixtures thereof.

Formulations for rectal or vaginal administration may be presented as asuppository, which may be prepared by mixing a subject composition withone or more suitable non-irritating excipients or carriers comprising,for example, cocoa butter, polyethylene glycol, a suppository wax or asalicylate, and which is solid at room temperature, but liquid at bodytemperature and, therefore, will melt in the body cavity and release theactive agent.

Dosage forms for transdermal administration of a subject compositioninclude powders, sprays, ointments, pastes, creams, lotions, gels,solutions, patches and inhalants. The active component may be mixedunder sterile conditions with a pharmaceutically acceptable carrier, andwith any preservatives, buffers, or propellants which may be required.

The ointments, pastes, creams and gels may contain, in addition to asubject composition, excipients, such as animal and vegetable fats,oils, waxes, paraffins, starch, tragacanth, cellulose derivatives,polyethylene glycols, silicones, bentonites, silicic acid, talc and zincoxide, or mixtures thereof.

Powders and sprays may contain, in addition to a subject composition,excipients such as lactose, talc, silicic acid, aluminum hydroxide,calcium silicates and polyamide powder, or mixtures of these substances.Sprays may additionally contain customary propellants, such aschlorofluorohydrocarbons and volatile unsubstituted hydrocarbons, suchas butane and propane.

Compositions and compounds of the present invention may alternatively beadministered by aerosol. This is accomplished by preparing an aqueousaerosol, liposomal preparation or solid particles containing thecompound. A non-aqueous (e.g., fluorocarbon propellant) suspension couldbe used. Sonic nebulizers may be used because they minimize exposing theagent to shear, which may result in degradation of the compoundscontained in the subject compositions. Ordinarily, an aqueous aerosol ismade by formulating an aqueous solution or suspension of a subjectcomposition together with conventional pharmaceutically acceptablecarriers and stabilizers. The carriers and stabilizers vary with therequirements of the particular subject composition, but typicallyinclude non-ionic surfactants (Tweens, Pluronics, or polyethyleneglycol), innocuous proteins like serum albumin, sorbitan esters, oleicacid, lecithin, amino acids such as glycine, buffers, salts, sugars orsugar alcohols. Aerosols generally are prepared from isotonic solutions.

Pharmaceutical compositions of this invention suitable for parenteraladministration comprise a subject composition in combination with one ormore pharmaceutically-acceptable sterile isotonic aqueous or non-aqueoussolutions, dispersions, suspensions or emulsions, or sterile powderswhich may be reconstituted into sterile injectable solutions ordispersions just prior to use, which may contain antioxidants, buffers,bacteriostats, solutes which render the formulation isotonic with theblood of the intended recipient or suspending or thickening agents.

Examples of suitable aqueous and non-aqueous carriers which may beemployed in the pharmaceutical compositions of the invention includewater, ethanol, polyols (such as glycerol, propylene glycol,polyethylene glycol, and the like), and suitable mixtures thereof,vegetable oils, such as olive oil, and injectable organic esters, suchas ethyl oleate and cyclodextrins. Proper fluidity may be maintained,for example, by the use of coating materials, such as lecithin, by themaintenance of the required particle size in the case of dispersions,and by the use of surfactants

In another aspect, the invention provides enteral pharmaceuticalformulations including a disclosed compound and an enteric material; anda pharmaceutically acceptable carrier or excipient thereof. Entericmaterials refer to polymers that are substantially insoluble in theacidic environment of the stomach, and that are predominantly soluble inintestinal fluids at specific pHs. The small intestine is the part ofthe gastrointestinal tract (gut) between the stomach and the largeintestine, and includes the duodenum, jejunum, and ileum. The pH of theduodenum is about 5.5, the pH of the jejunum is about 6.5 and the pH ofthe distal ileum is about 7.5. Accordingly, enteric materials are notsoluble, for example, until a pH of about 5.0, of about 5.2, of about5.4, of about 5.6, of about 5.8, of about 6.0, of about 6.2, of about6.4, of about 6.6, of about 6.8, of about 7.0, of about 7.2, of about7.4, of about 7.6, of about 7.8, of about 8.0, of about 8.2, of about8.4, of about 8.6, of about 8.8, of about 9.0, of about 9.2, of about9.4, of about 9.6, of about 9.8, or of about 10.0. Exemplary entericmaterials include cellulose acetate phthalate (CAP), hydroxypropylmethylcellulose phthalate (HPMCP), polyvinyl acetate phthalate (PVAP),hydroxypropyl methylcellulose acetate succinate (HPMCAS), celluloseacetate trimellitate, hydroxypropyl methylcellulose succinate, celluloseacetate succinate, cellulose acetate hexahydrophthalate, cellulosepropionate phthalate, cellulose acetate maleate, cellulose acetatebutyrate, cellulose acetate propionate, copolymer of methylmethacrylicacid and methyl methacrylate, copolymer of methyl acrylate,methylmethacrylate and methacrylic acid, copolymer of methylvinyl etherand maleic anhydride (Gantrez ES series), ethylmethyacrylate-methylmethacrylate-chlorotrimethylammonium ethyl acrylatecopolymer, natural resins such as zein, shellac and copal collophorium,and several commercially available enteric dispersion systems (e.g.,Eudragit L30D55, Eudragit FS30D, Eudragit L100, Eudragit S 100,Kollicoat EMM30D, Estacryl 30D, Coateric, and Aquateric). The solubilityof each of the above materials is either known or is readilydeterminable in vitro. The foregoing is a list of possible materials,but one of skill in the art with the benefit of the disclosure wouldrecognize that it is not comprehensive and that there are other entericmaterials that would meet the objectives of the present invention.

Advantageously, the invention also provides kits for use by a e.g. aconsumer in need of weight loss. Such kits include a suitable dosageform such as those described above and instructions describing themethod of using such dosage form to mediate, reduce or preventinflammation. The instructions would direct the consumer or medicalpersonnel to administer the dosage form according to administrationmodes known to those skilled in the art. Such kits could advantageouslybe packaged and sold in single or multiple kit units. An example of sucha kit is a so-called blister pack. Blister packs are well known in thepackaging industry and are being widely used for the packaging ofpharmaceutical unit dosage forms (tablets, capsules, and the like).Blister packs generally consist of a sheet of relatively stiff materialcovered with a foil of a preferably transparent plastic material. Duringthe packaging process recesses are formed in the plastic foil. Therecesses have the size and shape of the tablets or capsules to bepacked. Next, the tablets or capsules are placed in the recesses and thesheet of relatively stiff material is sealed against the plastic foil atthe face of the foil which is opposite from the direction in which therecesses were formed. As a result, the tablets or capsules are sealed inthe recesses between the plastic foil and the sheet. Preferably thestrength of the sheet is such that the tablets or capsules can beremoved from the blister pack by manually applying pressure on therecesses whereby an opening is formed in the sheet at the place of therecess. The tablet or capsule can then be removed via said opening.

It may be desirable to provide a memory aid on the kit, e.g., in theform of numbers next to the tablets or capsules whereby the numberscorrespond with the days of the regimen which the tablets or capsules sospecified should be ingested. Another example of such a memory aid is acalendar printed on the card, e.g., as follows “First Week, Monday,Tuesday, . . . etc. . . . Second Week, Monday, Tuesday, . . . ” etc.Other variations of memory aids will be readily apparent. A “daily dose”can be a single tablet or capsule or several pills or capsules to betaken on a given day. Also, a daily dose of a first compound can consistof one tablet or capsule while a daily dose of the second compound canconsist of several tablets or capsules and vice versa. The memory aidshould reflect this.

Also contemplated herein are methods and compositions that include asecond active agent, or administering a second active agent. Forexample, in addition to being overweight or obese, a subject or patientcan further have overweight- or obesity-related co-morbidities, i.e.,diseases and other adverse health conditions associated with,exacerbated by, or precipitated by being overweight or obese.Contemplated herein are disclosed compounds in combination with at leastone other agent that has previously been shown to treat theseoverweight- or obesity-related conditions.

For example, Type II diabetes has been associated with obesity. Certaincomplications of Type II diabetes, e.g., disability and premature death,can be prevented, ameliorated, or eliminated by sustained weight loss(Astrup, A. Pub Health Nutr (2001) 4:499-5 15). Agents administered totreat Type II diabetes include sulfonylureas (e.g., Chlorpropamide,Glipizide, Glyburide, Glimepiride); meglitinides (e.g., Repaglinide andNateglinide); biguanides (e.g., Metformin); thiazolidinediones(Rosiglitazone, Troglitazone, and Pioglitazone); dipeptidylpeptidase-4inhibitors (e.g., Sitagliptin, Vildagliptin, and Saxagliptin);glucagon-like peptide-1 mimetics (e.g., Exenatide and Liraglutide); andalpha-glucosidase inhibitors (e.g., Acarbose and Miglitol.

Cardiac disorders and conditions, for example hypertension,dyslipidemia, ischemic heart disease, cardiomyopathy, cardiacinfarction, stroke, venous thromboembolic disease and pulmonaryhypertension, have been linked to overweight or obesity. For example,hypertension has been linked to obesity because excess adipose tissuesecretes substances that are acted on by the kidneys, resulting inhypertension. Additionally, with obesity there are generally higheramounts of insulin produced (because of the excess adipose tissue) andthis excess insulin also elevates blood pressure. A major treatmentoption of hypertension is weight loss. Agents administered to treathypertension include Chlorthalidone; Hydrochlorothiazide; Indapamide,Metolazone; loop diuretics (e.g., Bumetanide, Ethacrynic acid,Furosemide, Lasix, Torsemide); potassium-sparing agents (e.g., Amiloridehydrochloride, benzamil, Spironolactone, and Triamterene); peripheralagents (e.g., Reserpine); central alpha-agonists (e.g., Clonidinehydrochloride, Guanabenz acetate, Guanfacine hydrochloride, andMethyldopa); alpha-blockers (e.g., Doxazosin mesylate, Prazosinhydrochloride, and Terazosin hydrochloride); beta-blockers (e.g.,Acebutolol, Atenolol, Betaxolol, Bisoprolol fumarate, Carteololhydrochloride, Metoprolol tartrate, Metoprolol succinate, Nadolol,Penbutolol sulfate, Pindolol, Propranolol hydrochloride, and Timololmaleate); combined alpha- and beta-blockers (e.g., Carvedilol andLabetalol hydrochloride); direct vasodilators (e.g., Hydralazinehydrochloride and Minoxidil); calcium antagonists (e.g., Diltiazemhydrochloride and Verapamil hydrochloride); dihydropyridines (e.g.,Amlodipine besylate, Felodipine, Isradipine, Nicardipine, Nifedipine,and Nisoldipine); ACE inhibitors (benazepril hydrochloride, Captopril,Enalapril maleate, Fosinopril sodium, Lisinopril, Moexipril, Quinaprilhydrochloride, Ramipril, Trandolapril); Angiotensin II receptor blockers(e.g., Losartan potassium, Valsartan, and Irbesartan); Renin inhibitors(e.g., Aliskiren); and combinations thereof. These compounds areadministered in regimens and at dosages known in the art.

Carr et al. (The Journal of Clinical Endocrinology & Metabolism (2004)Vol. 89, No. 6 2601-2607) discusses a link between being overweight orobese and dyslipidemia. Dyslipidemia is typically treated with statins.Statins, HMG-CoA reductase inhibitors, slow down production ofcholesterol in a subject and/or remove cholesterol buildup fromarteries. Statins include mevastatin, lovastatin, pravastatin,simvastatin, velostatin, dihydrocompactin, fluvastatin, atorvastatin,dalvastatin, carvastatin, crilvastatin, bevastatin, cefvastatin,rosuvastatin, pitavastatin, and glenvastatin. These compounds areadministered in regimens and at dosages known in the art. Eckel(Circulation (1997) 96:3248-3250) discusses a link between beingoverweight or obese and ischemic heart disease. Agents administered totreat ischemic heart disease include statins, nitrates (e.g., IsosorbideDinitrate and Isosorbide Mononitrate), beta-blockers, and calciumchannel antagonists. These compounds are administered in regimens and atdosages known in the art.

Wong et al. (Nature Clinical Practice Cardiovascular Medicine (2007)4:436-443) discusses a link between being overweight or obese andcardiomyopathy. Agents administered to treat cardiomyopathy includeinotropic agents (e.g., Digoxin), diuretics (e.g., Furosemide), ACEinhibitors, calcium antagonists, anti-arrhythmic agents (e.g., Sotolol,Amiodarone and Disopyramide), and beta-blockers. These compounds areadministered in regimens and at dosages known in the art. Yusef et al.(Lancet (2005) 366(9497):1640-1649) discusses a link between beingoverweight or obese and cardiac infarction. Agents administered to treatcardiac infarction include ACE inhibitors, Angiotensin II receptorblockers, direct vasodilators, beta blockers, anti-arrhythmic agents andthrombolytic agents (e.g., Alteplase, Retaplase, Tenecteplase,Anistreplase, and Urokinase). These compounds are administered inregimens and at dosages known in the art.

Suk et al. (Stroke (2003) 34:1586-1592) discusses a link between beingoverweight or obese and strokes. Agents administered to treat strokesinclude anti-platelet agents (e.g., Aspirin, Clopidogrel, Dipyridamole,and Ticlopidine), anticoagulant agents (e.g., Heparin), and thrombolyticagents. Stein et al. (The American Journal of Medicine (2005)18(9):978-980) discusses a link between being overweight or obese andvenous thromboembolic disease. Agents administered to treat venousthromboembolic disease include anti-platelet agents, anticoagulantagents, and thrombolytic agents. Sztrymf et al. (Rev Pneumol Clin (2002)58(2): 104-10) discusses a link between being overweight or obese andpulmonary hypertension. Agents administered to treat pulmonaryhypertension include inotropic agents, anticoagulant agents, diuretics,potassium (e.g., K-dur), vasodilators (e.g., Nifedipine and Diltiazem),Bosentan, Epoprostenol, and Sildenafil. Respiratory disorders andconditions such as obesity-hypoventilation syndrome, asthma, andobstructive sleep apnea, have been linked to being overweight or obese.Elamin (Chest (2004) 125:1972-1974) discusses a link between beingoverweight or obese and asthma. Agents administered to treat asthmainclude bronchodilators, anti-inflammatory agents, leukotriene blockers,and anti-Ige agents. Particular asthma agents include Zafirlukast,Flunisolide, Triamcinolone, Beclomethasone, Terbutaline, Fluticasone,Formoterol, Beclomethasone, Salmeterol, Theophylline, and Xopenex.

Kessler et al. (Eur Respir J (1996) 9:787-794) discusses a link betweenbeing overweight or obese and obstructive sleep apnea. Agentsadministered to treat sleep apnea include Modafinil and amphetamines.

Hepatic disorders and conditions, such as nonalcoholic fatty liverdisease, have been linked to being overweight or obese. Tolman et al.(Ther Clin Risk Manag (2007) 6:1153-1163) discusses a link between beingoverweight or obese and nonalcoholic fatty liver disease. Agentsadministered to treat nonalcoholic fatty liver disease includeantioxidants (e.g., Vitamins E and C), insulin sensitizers (Metformin,Pioglitazone, Rosiglitazone, and Betaine), hepatoprotectants, andlipid-lowering agents.

Skeletal disorders and conditions, such as, back pain and osteoarthritisof weight-bearing joints, have been linked to being overweight or obese.van Saase (J Rheumatol (1988) 15(7): 1152-1158) discusses a link betweenbeing overweight or obese and osteoarthritis of weight-bearing joints.Agents administered to treat osteoarthritis of weight-bearing jointsinclude Acetaminophen, non-steroidal anti-inflammatory agents (e.g.,Ibuprofen, Etodolac, Oxaprozin, Naproxen, Diclofenac, and Nabumetone),COX-2 inhibitors (e.g., Celecoxib), steroids, supplements (e.g.glucosamine and chondroitin sulfate), and artificial joint fluid.

Metabolic disorders and conditions, for example, Prader-Willi Syndromeand polycystic ovary syndrome, have been linked to being overweight orobese. Cassidy (Journal of Medical Genetics (1997) 34:917-923) discussesa link between being overweight or obese and Prader-Willi Syndrome.Agents administered to treat Prader-Willi Syndrome include human growthhormone (HGH), somatropin, and weight loss agents (e.g., Orlistat,Sibutramine, Methamphetamine, Ionamin, Phentermine, Bupropion,Diethylpropion, Phendimetrazine, Benzphetermine, and Topamax).

Hoeger (Obstetrics and Gynecology Clinics of North America (2001)28(1):85-97) discusses a link between being overweight or obese andpolycystic ovary syndrome. Agents administered to treat polycystic ovarysyndrome include insulin-sensitizers, combinations of synthetic estrogenand progesterone, Spironolactone, Eflomithine, and Clomiphene.Reproductive disorders and conditions such as sexual dysfunction,erectile dysfunction, infertility, obstetric complications, and fetalabnormalities, have been linked to being overweight or obese. Larsen etal. (Int J Obes (Lond) (2007) 8:1189-1198) discusses a link betweenbeing overweight or obese and sexual dysfunction. Chung et al. (Eur Urol(1999) 36(1):68-70) discusses a link between being overweight or obeseand erectile dysfunction. Agents administered to treat erectiledysfunction include phosphodiesterase inhibitors (e.g., Tadalafil,Sildenafil citrate, and Vardenafil), prostaglandin E analogs (e.g.,Alprostadil), alkaloids (e.g., Yohimbine), and testosterone. Pasquali etal. (Hum Reprod (1997) 1:82-87) discusses a link between beingoverweight or obese and infertility. Agents administered to treatinfertility include Clomiphene, Clomiphene citrate, Bromocriptine,Gonadotropin-releasing Hormone (GnRH), GnRH agonist, GnRH antagonist,Tamoxifen/nolvadex, gonadotropins, Human Chorionic Gonadotropin (HCG),Human Menopausal Gonadotropin (HmG), progesterone, recombinant folliclestimulating hormone (FSH), Urofollitropin, Heparin, Follitropin alfa,and Follitropin beta.

Weiss et al. (American Journal of Obstetrics and Gynecology (2004)190(4): 1091-1097) discusses a link between being overweight or obeseand obstetric complications. Agents administered to treat obstetriccomplications include Bupivacaine hydrochloride, Dinoprostone PGE2,Meperidine HCl, Ferro-folic-500/iberet-folic-500, Meperidine,Methylergonovine maleate, Ropivacaine HCl, Nalbuphine HCl, OxymorphoneHCl, Oxytocin, Dinoprostone, Ritodrine, Scopolamine hydrobromide,Sufentanil citrate, and Oxytocic.

Psychiatric disorders and conditions, for example, weight-associateddepression and anxiety, have been linked to being overweight or obese.Dixson et al. (Arch Intern Med (2003) 163:2058-2065) discusses a linkbetween being overweight or obese and depression. Agents administered totreat depression include serotonin reuptake inhibitors (e.g.,Fluoxetine, Escitalopram, Citalopram, Paroxetine, Sertraline, andVenlafaxine); tricyclic antidepressants (e.g., Amitriptyline, Amoxapine,Clomipramine, Desipramine, Dosulepin hydrochloride, Doxepin, Imipramine,Iprindole, Lofepramine, Nortriptyline, Opipramol, Protriptyline, andTrimipramine); monoamine oxidase inhibitors (e.g., Isocarboxazid,Moclobemide, Phenelzine, Tranylcypromine, Selegiline, Rasagiline,Nialamide, Iproniazid, Iproclozide, Toloxatone, Linezolid, Dienolidekavapyrone desmethoxyyangonin, and Dextroamphetamine); psychostimulants(e.g., Amphetamine, Methamphetamine, Methylphenidate, and Arecoline);antipsychotics (e.g., Butyrophenones, Phenothiazines, Thioxanthenes,Clozapine, Olanzapine, Risperidone, Quetiapine, Ziprasidone,Amisulpride, Paliperidone, Symbyax, Tetrabenazine, and Cannabidiol); andmood stabilizers (e.g., Lithium carbonate, Valproic acid, Divalproexsodium, Sodium valproate, Lamotrigine, Carbamazepine, Gabapentin,Oxcarbazepine, and Topiramate).

Simon et al. (Archives of General Psychiatry (2006) 63(7):824-830)discusses a link between being overweight or obese and anxiety. Agentsadministered to treat anxiety include serotonin reuptake inhibitors,mood stabilizers, benzodiazepines (e.g., Alprazolam, Clonazepam,Diazepam, and Lorazepam), tricyclic antidepressants, monoamine oxidaseinhibitors, and beta-blockers.

Another aspect of the invention provides methods for facilitating andmaintaining weight loss in a subject involving administering to thesubject an amount of a disclosed compound effective to result in weightloss in the subject; and administering a therapeutically effectiveamount of a different weight loss agent to maintain a reduced weight inthe subject. Weight loss agents include serotonin and noradrenergicre-uptake inhibitors; noradrenergic re-uptake inhibitors; selectiveserotonin re-uptake inhibitors; and intestinal lipase inhibitors.Particular weight loss agents include orlistat, sibutramine,methamphetamine, ionamin, phentermine, bupropion, diethylpropion,phendimetrazine, benzphetermine, bromocriptine, lorcaserin, topiramate,or agents acting to modulate food intake by blocking ghrelin action,inhibiting diacylglycerol acyltransferase 1 (DGAT1) activity, inhibitingstearoyl CoA desaturase 1 (SCD1) activity, inhibiting neuropeptide Yreceptor 1 function, activating neuropeptide Y receptor 2 or 4 function,or inhibiting activity of sodium-glucose cotransporters 1 or 2. Thesecompounds are administered in regimens and at dosages known in the art.

EXAMPLES

The compounds described herein can be prepared in a number of ways basedon the teachings contained herein and synthetic procedures known in theart. In the description of the synthetic methods described below, it isto be understood that all proposed reaction conditions, including choiceof solvent, reaction atmosphere, reaction temperature, duration of theexperiment and workup procedures, can be chosen to be the conditionsstandard for that reaction, unless otherwise indicated. It is understoodby one skilled in the art of organic synthesis that the functionalitypresent on various portions of the molecule should be compatible withthe reagents and reactions proposed. Substituents not compatible withthe reaction conditions will be apparent to one skilled in the art, andalternate methods are therefore indicated. The starting materials forthe examples are either commercially available or are readily preparedby standard methods from known materials.

At least some of the compounds identified as “Intermediates” herein arecontemplated as compounds of the invention.

¹H NMR spectra were recorded at ambient temperature using a Varian UnityInova (400 MHz) spectrometer with a triple resonance 5 mm probe forExample compounds, and either a Bruker Avance DRX (400 MHz) spectrometeror a Bruker Avance DPX (300 MHz) spectrometer for Intermediatecompounds. Chemical shifts are expressed in ppm relative totetramethylsilane. The following abbreviations have been used: br=broadsignal, s=singlet, d=doublet, dd=double doublet, ddd=double doubledoublet, dt=double triplet, t=triplet, td=triple doublet, q=quartet,m=multiplet.

Mass Spectrometry (LCMS) experiments to determine retention times andassociated mass ions were performed using the following methods:

Method A: Experiments were performed on a Waters ZMD LC quadrapole massspectrometer linked to a Waters 1525 LC system with a diode arraydetector. The spectrometer has an electrospray source operating inpositive and negative ion mode. Additional detection was achieved usinga Sedex 85 evaporative light scattering detector. LC was carried outusing a Luna 3 micron 30×4.6 mm C18 column and a 2 mL/minute flow rate.The initial solvent system was 95% water containing 0.1% formic acid(solvent A) and 5% acetonitrile containing 0.1% formic acid (solvent B)for the first 0.5 minute followed by a gradient up to 5% solvent A and95% solvent B over the next 4 minutes. The final solvent system was heldconstant for a further 1 minute.

Method B: Experiments were performed on a Waters V G Platform quadrupolespectrometer linked to a Hewlett Packard 1050 LC system with a diodearray detector. The spectrometer has an electrospray source operating inpositive and negative ion mode. Additional detection was achieved usinga Sedex 85 evaporative light scattering detector. LC was carried outusing a Luna 3 micron 30×4.6 mm C18 column and a 2 mL/minute flow rate.The initial solvent system was 95% water containing 0.1% formic acid(solvent A) and 5% acetonitrile containing 0.1% formic acid (solvent B)for the first 0.3 minute followed by a gradient up to 5% solvent A and95% solvent B over the next 4 minutes. The final solvent system was heldconstant for a further 1 minute.

Method C: Experiments were performed on a Waters Micromass ZQ2000quadrapole mass spectrometer linked to a Waters Acquity UPLC system witha PDA UV detector. The spectrometer has an electrospray source operatingin positive and negative ion mode. LC was carried out using an AcquityBEH 1.7 micron C18 column, an Acquity BEH Shield 1.7 micron RP18 columnor an Acquity HSST 1.8 micron column. Each column has dimensions of100×2.1 mm and was maintained at 40° C. with a flow rate of 0.4mL/minute. The initial solvent system was 95% water containing 0.1%formic acid (solvent A) and 5% acetonitrile containing 0.1% formic acid(solvent B) for the first 0.4 minute followed by a gradient up to 5%solvent A and 95% solvent B over the next 6 minutes. The final solventsystem was held constant for a further 0.8 minutes.

Method D: Experiments were performed on a Shimadzu LCMS-2020spectrometer with an electrospray source operating in positive ion mode.LC was carried out using a Shimadzu Shim-pack XR-ODS 2.2 micron 50×3.0mm column. The initial solvent system was 95% water containing 0.05%trifluoroacetic acid (solvent A) and 5% acetonitrile (solvent B) for thefirst 0.01 minute then a gradient up to 100% solvent B over the next 1.3minutes. The final solvent system was held constant for a further 1minute.

Method E: Experiments were performed on a Waters ZMD LC quadrapole massspectrometer linked to a Hewlett Packard HD 1100 system with a diodearray detector. The spectrometer has an electrospray source operating inpositive and negative ion mode. LC was carried out using a Luna 3 micron30×4.6 mm C18 column and a 2 mL/minute flow rate. The initial solventsystem was 95% water containing 0.1% formic acid (solvent A) and 5%acetonitrile containing 0.1% formic acid (solvent B) for the first 0.5minute followed by a gradient up to 5% solvent A and 95% solvent B overthe next 4 minutes. The final solvent system was held constant for afurther 1 minute.

Method F: Experiments were performed on a Waters V G Platform quadrupolespectrometer linked to a Hewlett Packard 1050 LC system with a diodearray detector. The spectrometer has an electrospray source operating inpositive and negative ion mode. Additional detection was achieved usinga Sedex 85 evaporative light scattering detector. LC was carried outusing a Luna 3 micron 30×4.6 mm C18 column and a 2 mL/minute flow rate.The initial solvent system was 95% water containing 0.1% formic acid(solvent A) and 5% acetonitrile containing 0.1% formic acid (solvent B)for the first 0.3 minute followed by a gradient up to 5% solvent A and95% solvent B over the next 4 minutes. The final solvent system was heldconstant for a further 1 minute. Microwave experiments were carried outusing a Biotage Initiator™, which uses a single-mode resonator anddynamic field tuning. Temperatures from 40-250° C. can be achieved, andpressures of up to 20 bars can be reached. A facility exists to applyair cooling during the irradiation.

Preparative HPLC purification was carried out using either aC18-reverse-phase column from Genesis (C18) or a C6-phenyl column fromPhenomenex (C6-phenyl) (100×22.5 mm i.d. with 7 micron particle size, UVdetection at 230 or 254 nm, flow 5-15 mL/min), eluting with gradientsfrom 100-0 to 0-100% water/acetonitrile or water/methanol containing0.1% formic acid. Fractions containing the required product (identifiedby LCMS analysis) were pooled, the organic fraction removed byevaporation, and the remaining aqueous fraction lyophilised, to give theproduct.

Compounds which required column chromatography were purified manually orfully automatically using either a Biotage SP1™ Flash Purificationsystem with Touch Logic Control™ or a Combiflash Companion® withpre-packed silica gel Isolute® SPE cartridge, Biotage SNAP cartridge orRedisep® Rf cartridge respectively.

Compounds have been named using Autonom2000 within ISISDraw.

Abbreviations:

-   -   DCM Dichloromethane    -   IMS Industrial methylated spirits    -   DMF N,N-Dimethylformamide    -   DMAP 4-Dimethylaminopyridine    -   THF Tetrahydrofuran    -   DMSO Dimethylsulfoxide    -   NMP N-methylpyrrolidinone    -   DCE 1,2-Dichloroethane    -   HATU 7-Azabenzotriazol-1-yl-N,N,N′,N′,tetramethyluronium        hexafluorophosphate    -   EDAC N-(3-Dimethylaminopropyl)-N′ethylcarbodiimide hydrochloride    -   IMS Industrial methylated spirit    -   NMM N-methylmorpholine    -   DBU 1,8-Diazabicyclo[5.4.0]undec-7-ene

Example 1Cis-(3aRS,9bRS)-7-(Benzenesulfonylamino)-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylicacid

Lithium hydroxide (0.048 g) was added to a solution of methylcis-(3aRS,9bRS)-7-(benzenesulfonylamino)-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate(Intermediate 1, 0.08 g) in a mixture of dioxane (10 mL) and water (5mL) and the resultant mixture was irradiated in the microwave at 110° C.with air cooling for 20 minutes. Further lithium hydroxide (0.2 g) wasadded and the mixture was irradiated in the microwave at 110° C. withair cooling for a total of 80 minutes. After cooling, the solution wasacidified by addition of aqueous formic acid solution (10%) and theresultant mixture was extracted with ethyl acetate, dried (MgSO₄) andfiltered. The filtrate was evaporated to dryness. The residue wasdissolved in a mixture of methanol (10 mL) and water (5 mL) and treatedwith lithium hydroxide (0.2 g) then irradiated in the microwave at 110°C. with air cooling for 40 minutes. After cooling, the solution wasacidified by addition of formic acid (10%) and the resultant mixture wasextracted with ethyl acetate, dried (MgSO₄) and filtered. The filtratewas evaporated to dryness and the residue was purified by preparativeHPLC (C18) eluting with a mixture of acetonitrile and water, containing0.1% formic acid, with a gradient of 30-50% to givecis-(3aRS,9bRS)-7-(benzenesulfonylamino)-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylicacid (0.019 g) as a white solid.

¹H NMR (CD₃OD) δ: 7.71 (2H, d), 7.54 (1H, t), 7.44 (2H, t), 7.24 (1H,d), 7.12 (1H, d), 4.24 (1H, m), 4.09 (1H, dd), 3.92 (1H, dd), 3.8-3.65(2H, m), 3.47 (1H, m), 2.45 (1H, m), 1.83 (1H, m).

LCMS (Method C) r/t 3.79 (M−H) 374.

Example 2Cis-(3aRS,9bRS)-7-[2-(3-Diethylaminopropyl)-4-fluorobenzenesulfonyl-amino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylicacid

A solution of7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylicacid (Intermediate 8, 0.1 g) in a mixture of IMS (2 mL) and glacialacetic acid (3 mL) was treated, under an atmosphere of nitrogen, withpalladium hydroxide on carbon (10%, 0.02 g). The nitrogen was replacedby hydrogen and the mixture was stirred under an atmosphere of hydrogenfor 100 minutes. The mixture was filtered through Celite and thefiltrate was evaporated to dryness. The residue was dissolved in tolueneand the solution was re-evaporated. The residue was triturated withether and the solid was collected by filtration and purified bypreparative HPLC (C6-phenyl) eluting with a mixture of acetonitrile andwater, containing 0.1% formic acid, with a gradient of 20-40% to givecis-(3aRS,9bRS)-7-[2-(3-diethylaminopropyl-4-fluorobenzenesulfonyl-amino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylicacid (0.1 g) as a white solid.

¹H NMR (CD₃OD) δ: 7.94 (1H, dd), 7.18 (1H, d), 7.17 (1H, m), 7.06 (1H,d), 6.99 (1H, dt), 4.21 (1H, m), 3.98 (1H, dd), 3.88 (1H, dd), 3.72 (2H,m), 3.42 (1H, m), 3.23 (6H, m), 3.10 (2H, m), 2.42 (1H, m), 1.98 (2H,m), 1.81 (1H, m), 1.31 (6H, t).

LCMS (Method C) r/t 3.10 (M+H) 507.

Example 3Cis-(3aRS,9bRS)-7-[2-(3-{Pyrrolidin-1-yl}propyl)-4-fluorobenzene-sulfonylamino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylicacid

Lithium hydroxide (0.028 g) was added to a solution of methylcis-(3aRS,9bRS)-7-[2-(3-{pyrrolidin-1-yl}propyl)-4-fluorobenzenesulfonylamino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate(Intermediate 14, 0.06 g) in dioxane (2 mL) and water (1 mL) and themixture was stirred and heated at 80° C. for 8 hours. After cooling, themixture was acidified by addition of aqueous formic acid solution (10%)and extracted with DCM. The organic layer was dried (MgSO₄) andfiltered. The filtrate was evaporated to dryness and the residue waspurified by chromatography on silica eluting with a mixture of ammoniain methanol (2M) and DCM with a gradient of 1-10%. The isolated solidwas triturated with a mixture of ether and cyclohexane (50%) and thesolid was collected by filtration. The solid was purified by preparativeHPLC (C18) eluting with a mixture of acetonitrile and water, containing0.1% formic acid, with a gradient of 10-95%. The isolated product wastriturated with ether and the solid was collected by filtration to givecis-(3aRS,9bRS)-7-[2-(3-{pyrrolidin-1-yl}propyl)-4-fluorobenzenesulfonylamino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylicacid (0.006 g) as a white solid.

¹H NMR (CD₃OD) δ: 7.93 (1H, dd), 7.21 (1H, d), 7.14 (1H, dd), 7.08 (1H,d), 6.99 (1H, dt), 4.21 (1H, m), 3.98 (1H, dd), 3.88 (1H, dd), 3.72 (2H,m), 3.43 (2H, m), 3.30 (4H, m), 3.13 (3H, m), 2.42 (1H, m), 2.07 (4H,m), 2.0 (2H, m), 1.81 (1H, m).

LCMS (Method C) r/t 3.11 (M+H) 505.

Example 4Cis-(3aRS,9bRS)-7-[2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluoro-benzenesulfonylamino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylicacid

Prepared by proceeding in a similar manner to Example 3, starting frommethylcis-(3aRS,9bRS)-7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate(Intermediate 17) and heating at 80° C. overnight.

¹H NMR (DMSO-d₆) δ: 7.65 (1H, dd), 7.30 (1H, d), 7.19 (2H, m), 7.02 (1H,d), 6.92 (1H, d), 6.10 (1H, m), 4.09 (1H, m), 3.82-3.64 (4H, m),3.63-3.30 (3H, m), 3.03 (4H, q), 2.35 (1H, m), 1.68 (1H, m), 1.07 (6H,t).

LCMS (Method C) r/t 3.05 (M+H) 505.

Examples 5 and 6 Separation of Enantiomers from Example 4

Sample from Example 4 was subjected to chiral separation using aChiralPak IC column, 4.6 mm×250 mm, particle size 5 micron. Injectionsolvent DCE:absolute ethanol 1:1, injection concentration 1 mg/100 μL,injection volume 120 μL. Eluting solvent absolute ethanol, flow rate0.55 mL/minute, temperature 21° C.

Example 5 First Eluting Enantiomer: Retention Time on Above Column:34.96 Minutes, 93% De

¹H NMR (DMSO-d₆) δ: 7.64 (1H, dd), 7.29 (1H, d), 7.18 (2H, m), 7.01 (1H,d), 6.92 (1H, d), 6.08 (1H, m), 4.09 (1H, m), 3.75 (2H, m), 3.59 (2H,m), 3.33 (3H, m), 3.03 (4H, br), 2.34 (1H, m), 1.68 (1H, m), 1.06 (6H,t).

LCMS (Method C) r/t 3.07 (M+H) 505.

Example 6 Second Eluting Enantiomer: Retention Time on Above Column40.97 Minutes, 65% De

¹H NMR (DMSO-d₆) δ: 7.64 (1H, dd), 7.29 (1H, d), 7.18 (2H, m), 7.01 (1H,d), 6.92 (1H, d), 6.08 (1H, m), 4.09 (1H, m), 3.75 (2H, m), 3.59 (2H,m), 3.33 (3H, m), 3.03 (4H, br), 2.34 (1H, m), 1.68 (1H, m), 1.06 (6H,t).

LCMS (Method C) r/t 3.06 (M+H) 505.

Example 77-[2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,2-dihydrofuro[2,3-c]quinoline-6-carboxylicacid formate salt

Prepared by proceeding in a similar manner to Example 1, starting frommethyl7-[N-{2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl)}-N-(methoxy-carbonyl)amino]-1,2-dihydrofuro[2,3-c]quinoline-6-carboxylate(Intermediate 20) as a yellow solid.

¹H NMR (CD₃OD) δ: 8.50 (1H, s), 8.47 (2H, s), 7.96 (1H, m), 7.91 (1H,d), 7.79 (1H, d), 7.45 (1H, d), 7.11 (2H, m), 6.13 (1H, m), 3.79 (2H,d), 3.59 (2H, t), 3.10 (6H, m), 1.16 (6H, m).

LCMS (Method C) r/t 2.84 (M+H) 500.

Example 87-(Benzenesulfonylamino)-1,2-dihydrofuro[2,3-c]quinoline-6-carboxylicacid formate salt

Prepared by proceeding in a similar manner to Example 1, starting frommethyl7-(benzenesulfonylamino)-1,2-dihydrofuro[2,3-c]quinoline-6-carboxylate(Intermediate 26).

¹H NMR (DMSO-d₆) δ: 8.54 (1H, s), 8.25 (1H, s), 7.78 (3H, m), 7.66 (1H,d), 7.44 (3H, m), 4.69 (2H, t), 3.46 (2H, t).

LCMS (Method C) r/t 3.66 (M+H) 371.

Example 9Cis-(3aRS,9bRS)-7-[2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,2,3a,4,5,9b-hexahydrofuro[2,3-c]quinoline-6-carboxylicacid

Lithium hydroxide (0.09 g) was added to a solution of methylcis-(3aRS,9bRS)-5-acetyl-7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,2,3a,4,5,9b-hexahydrofuro[2,3-c]quinoline-6-carboxylate(Intermediate 27, 0.06 g) in a mixture of dioxane (5 mL) and water (1mL) and the mixture was stirred and heated at 80° C. overnight. Themixture was then irradiated in the microwave at 150° C. for 30 minutesand then at 180° C. for 30 minutes. After cooling, the mixture wasfiltered and the filtrate was acidified by addition of formic acid (1mL) and then evaporated to dryness. The residue was purified bypreparative HPLC (C18) eluting with a mixture of acetonitrile and water,containing 0.1% formic acid, with a gradient of 10-98%. The isolatedproduct was dissolved in DCM and evaporated to dryness then dissolved inether and evaporated to dryness to givecis-(3aRS,9bRS)-7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,2,3a,4,5,9b-hexahydrofuro[2,3-c]quinoline-6-carboxylicacid (0.005 g) as a white solid.

¹H NMR (CDCl₃) δ: 8.54 (1H, br s), 7.99 (1H, br s), 7.48 (1H, d), 7.04(1H, m), 6.90 (1H, d), 6.76 (1H, d), 6.62 (1H, m), 6.11 (1H, m), 4.17(1H, m), 3.82 (1H, m), 3.78-3.59 (2H, m), 3.32-3.10 (4H, m), 3.04-2.86(3H, m), 2.35 (1H, m), 1.79 (1H, m), 1.15 (6H, t).

LCMS (Method C) r/t 3.31 (M+H) 504

Example 10(1aRS,7bSR)-5-[2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Methyl(1aRS,7bSR)-5-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 40, 0.185 g) and lithium hydroxide monohydrate (0.159 g)were suspended in dioxane (4 mL) and water (1 mL). The reaction mixturewas irradiated in the microwave at 135° C. for 30 minutes. Aftercooling, the mixture was acidified to pH4 with formic acid, then ethanoland toluene were added and the mixture concentrated in vacuo. Theresidue was triturated with a mixture of methanol and DCM (10%) and thesolid was filtered off and washed with a mixture of methanol and DCM.The filtrate was concentrated in vacuo and the residue was purified bychromatography on silica, eluting with a mixture of methanol and DCMwith a gradient of 0-8%. The resultant product was triturated with ethylacetate and dried in vacuo at 50° C. to give(1aRS,7bSR)-5-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.066 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.64 (1H, dd), 7.35 (1H, d), 7.27-7.19 (2H, m), 7.10(1H, d), 6.93 (1H, d), 6.20-6.10 (1H, m), 4.17 (1H, d), 3.76 (2H, br,s), 3.57 (1H, d), 3.10 (4H, br, q), 1.92 (1H, td), 1.75-1.69 (1H, m),1.13 (6H, t), 0.94 (1H, td), 0.74 (1H, m).

LCMS (Method C) r/t 3.32 (M+H) 475

Examples 11 and 12 Separation of Enantiomers from Example 10

Sample from Example 10 was subjected to chiral separation using aChiralPak IC column, 10 mm×250 mm, particle size 5 micron. Elutingsolvent tert-butyl methyl ether:isopropanol:DCM (16:20:64).

Example 11 First Eluting Enantiomer: r/t on Analytical Column (4.6mm×250 mm): 21.8 minutes >99% ee:(1aS,7bR)-5-[2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

¹H NMR (CDCl₃) δ: 7.63 (1H, d), 7.43 (1H, m), 7.15-7.08 (2H, m), 6.85(1H, dt), 6.72 (1H, dd), 5.93 (1H, m), 4.27 (1H, d), 3.98 (1H, br m),3.68 (1H, m), 3.58 (1H, br), 3.27-3.06 (4H, m), 1.87 (1H, m), 1.63 (1H,m), 1.23 (6H, t), 1.04 (1H, m), 0.91 (1H, m).

LCMS (Method C) r/t 3.30 (M+H) 475

Example 12 Second Eluting Enantiomer: r/t on Analytical Column (4.6mm×250 mm): 27.5 minutes, >99% ee:(1aR,7bS)-5-[2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

¹H NMR (CDCl₃) δ: 7.63 (1H, d), 7.43 (1H, m), 7.15-7.08 (2H, m), 6.85(1H, dt), 6.72 (1H, dd), 5.93 (1H, m), 4.27 (1H, d), 3.98 (1H, br m),3.68 (1H, m), 3.58 (1H, br), 3.27-3.06 (4H, m), 1.87 (1H, m), 1.63 (1H,m), 1.23 (6H, t), 1.04 (1H, m), 0.91 (1H, m).

LCMS (Method C) r/t 3.32 (M+H) 475.

Absolute configuration of Examples 11 and 12 determined by X-ray crystalanalysis of Example 12 with MetAP2.

Example 13(1aRS,7bSR)-5-[2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-7b-methyl-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a similar manner to Example 3, starting frommethyl(1aRS,7bSR)-5-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-7b-methyl-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 48).

¹H NMR (CDCl₃) δ: 9.8-9.2 (1H, br s), 7.65 (1H, d), 7.39 (1H, m), 7.24(1H, d), 7.18 (1H, d), 6.83 (1H, dt), 6.72 (1H, dd), 5.91 (1H, m), 4.21(1H, d), 3.98 (1H, br t), 3.71 (1H, d), 3.61 (1H, br s), 3.28-3.06 (4H,m), 1.41 (3H, s), 1.37 (1H, m), 1.24 (6H, t), 1.14 (1H, t), 0.74 (1H,dd).

LCMS (Method C) r/t 3.55 (M+H) 489.

Example 14(1aRS,7bSR)-5-[2-((E)-3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-7b-methyl-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Isolated as a minor by-product by preparative HPLC from the preparationof Example 13.

¹H NMR (CDCl₃) δ: 11.9 (1H, br s), 7.93 (1H, dd), 7.70 (1H, d), 7.25(1H, d), 7.10 (1H, d), 7.06 (1H, dd), 6.90 (1H, dt), 6.19 (1H, m), 4.23(1H, d), 3.76 (1H, d), 3.68 (2H, m), 3.29 (4H, q), 1.36 (6H, t), 1.35(3H, s), 1.31 (1H, m), 1.10 (1H, t), 1.67 (1H, dd).

LCMS (Method C) r/t 3.66 (M+H) 489.

Example 15Cis-(3aRS,9bRS)-7-[2-(4-dimethylaminobutylamino)benzenesulfonylamino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylicacid

4-Dimethylaminobutylamine (0.348 g) and triethylamine (0.2 ml) wereadded to a suspension ofcis-(3aRS,9bRS)-7-(2-fluorobenzenesulfonylamino)-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylicacid (Intermediate 57, 0.15 g) in acetonitrile (1.5 mL) and the mixturewas heated at 130° C. in a sealed tube for 36 hours. The mixture wasthen diluted with water (2 mL) and the solution was purified bypreparative HPLC (C6-phenyl) eluting with a mixture of methanol andwater, containing 0.1% formic acid, with a gradient of 5-98%. Theisolated product was further purified by chromatography on silicaeluting with a mixture of methanol and DCM with a gradient of 0-15% togivecis-(3aRS,9bRS)-7-[2-(4-dimethylaminobutylamino)-benzenesulfonylamino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylicacid (0.062 g) as a glass foam.

¹H NMR (CDCl₃) δ: 11.21 (1H, br s), 7.72 (1H, dd), 7.37 (1H, d), 7.26(1H, m), 7.02 (1H, d), 6.59 (1H, d), 6.56 (1H, t), 5.85 (1H, t), 4.29(1H, dt), 4.05 (1H, dd), 3.85 (1H, m), 3.77 (2H, m), 3.34 (1H, q), 3.21(2H, m), 2.98 (2H, t), 2.80 (6H, s), 2.41 (1H, m), 2.05 (1H, m), 1.83(1H, m), 1.71 (2H, m).

LCMS (Method C) r/t 3.18 (M+H) 490

Example 16(1aR,7bS)-5-[2-(3-Diethylaminopropyl)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a similar manner to Example 2, starting from(1aR,7bS)-5-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]-chromene-4-carboxylicacid (Example 12)

¹H NMR (CDCl₃) δ: 7.81 (1H, dd), 7.31 (1H, d), 7.07 (1H, d), 6.82 (2H,m), 4.32 (1H, d), 3.74 (1H, d), 3.42-3.32 (1H, m), 3.18 (4H, m),3.14-2.94 (3H, m), 2.00 (2H, m), 1.84 (1H, m), 1.62 (1H, m), 1.31 (6H,t), 1.04 (1H, m), 0.88 (1H, m).

LCMS (Method C) r/t 3.36 (M+H) 477.

Example 17(1aRS,7bSR)-5-[2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzene-sulfonylamino]-1,1-difluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a similar manner to Example 10, starting frommethyl(1aRS,7bSR)-5-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,1-difluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 59) as a white solid.

¹H NMR (CDCl₃) δ: 10.0-9.6 (1H, br s), 7.64 (1H, d), 7.47 (1H, dd), 7.21(1H, d), 7.13 (1H, d), 6.87 (1H, dt), 6.73 (1H, dd), 5.95 (1H, m), 4.28(1H, d), 3.96 (1H, m), 3.92-3.79 (1H, br s), 3.78-3.67 (1H, br s), 3.17(4H, q), 2.64 (1H, t), 2.23 (1H, m), 1.24 (6H, t).

LCMS (Method C) r/t 3.38 (M+H) 511.

Examples 18 and 19 Separation of Enantiomers from Example 17

Sample from Example 17 was subjected to chiral separation using aChiralPak IA column, 20 mm×250 mm, particle size 5 micron. Elutingsolvent methanol:ethanol:heptane (12.5:12.5:75).

Example 18 First Eluting Enantiomer: r/t on Analytical Column (4.6mm×250 mm): 14.7 Minutes >95% Ee

¹H NMR (DMSO-d₆) δ: 7.83 (1H, t), 7.27-7.17 (3H, m), 7.09 (1H, d), 6.85(1H, d), 5.98 (1H, m), 4.27 (1H, d), 3.76 (1H, m), 3.56 (1H, t), 2.90(1H, t), 2.85 (1H, t), 2.77 (4H, br s), 2.55 (1H, s), 0.97 (6H, br t).

LCMS (Method C) r/t 3.39 (M+H) 511

Example 19 Second Eluting Enantiomer: r/t on Analytical Column 19.0Minutes, >95% Ee

¹H NMR (DMSO-d₆) δ: 7.72 (1H, dd), 7.36 (1H, d), 7.26 (1H, dt), 7.21(1H, dd), 7.18 (1H, d), 6.99 (1H, d), 6.13 (1H, m), 4.29 (1H, d),3.87-3.70 (3H, m), 3.10 (4H, m), 2.96 (1H, t), 2.56 (1H, m), 1.11 (6H,t).

LCMS (Method C) r/t 3.39 (M+H) 511.

Example 20(1aRS,7bSR)-5-[2((Z)-3-Ethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of methyl(1aRS,7bSR)-5-[2((Z)-3-ethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 63, 0.09 g) and lithium hydroxide monohydrate (0.047 g) ina mixture of dioxane (10 mL) and water (5 mL) was stirred and heated at120° C. for 32 hours. After cooling, the mixture was concentrated undervacuum and the residue was acidified to pH4 with formic acid. Theresultant solid was collected by filtration and washed with water togive(1aRS,7bSR)-5-[2((Z)-3-ethylaminoprop-1-enyl)-4-fluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid (0.029 g) as a grey solid.

¹H NMR (DMSO-d₆) δ: 10.4-9.95 (1H, br s), 7.51 (1H, dd), 7.21 (1H, d),7.17 (1H, dt), 7.11 (1H, dd), 7.07 (1H, d), 6.99 (1H, d), 5.93 (1H, m),4.11 (1H, d), 3.60 (2H, m), 3.51 (1H, d), 2.92 (2H, q), 1.87 (1H, m),1.67 (1H, m), 1.12 (3H, t), 0.89 (1H, m), 0.69 (1H, m).

LCMS (Method C) r/t 3.32 (M+H) 447.

Examples 21 and 22 Separation of Enantiomers from Example 20

Sample from Example 20 was subjected to chiral separation using aChiralPak IC column, 10 mm×250 mm, particle size 5 micron. Elutingsolvent tert-butyl methyl ether:isopropanol:DCM (15:20:65).

Example 21 First Eluting Enantiomer: r/t on Analytical Column (4.6mm×250 mm): 14.3 Minutes >99% Ee

¹H NMR (DMSO-d₆) δ: 10.16 (2H, br s), 7.56 (1H, dd), 7.26 (1H, d), 7.22(1H, dt), 7.17 (1H, dd), 7.12 (1H, d), 7.05 (1H, d), 5.99 (1H, m), 4.16(1H, d), 3.65 (2H, m), 3.57 (1H, d), 2.98 (2H, q), 1.93 (1H, m), 1.73(1H, m), 1.17 (3H, t), 0.94 (1H, m), 0.78 (1H, q).

LCMS (Method C) r/t 3.27 (M+H) 447.

Example 22 Second Eluting Enantiomer: r/t on Analytical Column 20.6Minutes, >99% Ee

¹H NMR (DMSO-d₆) δ: 10.16 (2H, br s), 7.56 (1H, dd), 7.26 (1H, d), 7.22(1H, dt), 7.17 (1H, dd), 7.12 (1H, d), 7.05 (1H, d), 5.99 (1H, m), 4.16(1H, d), 3.65 (2H, m), 3.57 (1H, d), 2.98 (2H, q), 1.93 (1H, dt), 1.73(1H, m), 1.17 (3H, t), 0.94 (1H, dt), 0.75 (1H, q).

LCMS (Method C) r/t 3.26 (M+H) 447.

Example 23 (1aRS,7bSR)-5-{2[(Z)-3-(Pyrrolidin-1-yl)prop-1-enyl]-4-fluorobenzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a similar manner to Example 20, starting frommethyl(1aRS,7bSR)-5-{2[(Z)-3-(pyrrolidin-1-yl)prop-1-enyl]-4-fluorobenzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 66) as a white solid.

¹H NMR (DMSO-d₆) δ: 12.2-11.6 (1H, br s), 7.49 (1H, dd), 7.30 (1H, d),7.21-7.12 (2H, m), 7.09 (1H, m), 6.97 (1H, d), 6.10 (1H, m), 4.12 (1H,d), 3.80 (2H, d), 3.51 (1H, d), 3.28 (4H, m), 1.89 (1H, m), 1.85 (4H,m), 1.68 (1H, m), 0.90 (1H, m), 0.69 (1H, m).

LCMS (Method C) r/t 3.39 (M+H) 473

Examples 24 and 25 Separation of Enantiomers from Example 23

Sample from Example 23 was subjected to chiral separation using aChiralPak IC column, 10 mm×250 mm, particle size 5 micron. Elutingsolvent tert-butyl methyl ether:ethanol (75:25).

Example 24 First Eluting Enantiomer: r/t on Analytical Column (4.6mm×250 mm): 17.5 Minutes >99% Ee

¹H NMR (DMSO-d₆) δ: 7.55 (1H, dd), 7.35 (1H, d), 7.22 (2H, m), 7.14 (1H,d), 7.02 (1H, d), 6.14 (1H, m), 4.17 (1H, d), 3.84 (2H, br d), 3.57 (1H,d), 3.30 (4H, br), 1.97-1.85 (5H, br m), 1.73 (1H, m), 0.95 (1H, dt),0.74 (1H, q).

LCMS (Method C) r/t 3.33 (M+H) 473

Example 25 Second Eluting Enantiomer: r/t on Analytical Column 21.4Minutes, >98% Ee

¹H NMR (DMSO-d₆) δ: 7.55 (1H, dd), 7.34 (1H, d), 7.24 (1H, dd), 7.19(1H, dd), 7.14 (1H, d), 7.02 (1H, d), 6.14 (1H, dt), 4.17 (1H, d), 3.84(2H, br d), 3.57 (1H, d), 3.29 (4H, br), 1.97-1.85 (5H, br m), 1.73 (1H,m), 0.95 (1H, dt), 0.74 (1H, q).

LCMS (Method C) r/t 3.34 (M+H) 473.

Example 26(1aRS,7bSR)-5-[2-(3-Dimethylaminopropylamino)benzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of(1aRS,7bSR)-5-(2-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid (Intermediate 67, 0.15 g), 3-dimethylaminopropylamine (1.26 g) andtriethylamine (0.62 g) in NMP (6 mL) was stirred and heated at 140° C.for 48 hours. After cooling, the mixture was concentrated under vacuumand the residue was purified by chromatography on silica, eluting with amixture of methanol and DCM with a gradient of 5-10%. The resultantproduct was repurified by preparative TLC, eluting with a mixture ofmethanol and DCM (10%) to give(1aRS,7bSR)-5-[2-(3-dimethylaminopropylamino)-benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.08 g) as an off white solid.

¹H NMR (DMSO-d₆) δ: 7.36 (1H, dd), 7.22 (1H, dt),7.02 (2H, s), 6.68 (1H,d), 6.44 (1H, t), 6.24 (1H, br s), 4.11 (1H, d), 3.51 (1H, d), 3.30-3.10(4H, m), 2.68 (6H, s), 1.83 (1H, m), 1.72-1.52 (3H, m), 0.85 (1H, m),0.65 (1H, m).

LCMS (Method C) r/t 3.31 (M+H) 446.

Examples 27 and 28 Separation of Enantiomers from Example 26

Sample from Example 26 was subjected to chiral separation using aChiralPak IB column 20 mm×250 mm, particle size 5 micron. Elutingsolvent hexane:ethanol:diethylamine (49.8:50:0.2).

Example 27 First Eluting Enantiomer: r/t on Analytical Column (4.6mm×250 mm) 14.61 Minutes (>98% Ee)

¹H NMR (DMSO-d₆) δ: 7.37 (1H, dd), 7.23 (1H, dt),7.02 (2H, s), 6.68 (1H,d), 6.45 (1H, t), 6.24 (1H, br s), 4.11 (1H, d), 3.52 (1H, d), 3.35-3.02(4H, m), 2.67 (6H, s), 1.84 (1H, m), 1.74-1.52 (3H, m), 0.85 (1H, m),0.66 (1H, m).

LCMS (Method C) r/t 3.21 (M+H) 446.

Example 28 Second Eluting Enantiomer: r/t on Analytical Column (4.6mm×250 mm) 18.16 Minutes (>98% Ee)

¹H NMR (DMSO-d₆) δ: 7.37 (1H, dd), 7.23 (1H, dt),7.02 (2H, s), 6.68 (1H,d), 6.44 (1H, t), 6.25 (1H, br s), 4.11 (1H, d), 3.51 (1H, d), 3.41-3.05(4H, m), 2.69 (6H, s), 1.84 (1H, m), 1.74-1.52 (3H, m), 0.85 (1H, m),0.66 (1H, m).

LCMS (Method C) r/t 3.20 (M+H) 446.

Example 29(1aRS,7bSR)-5-[2-(4-Dimethylaminobutylamino)benzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a similar manner to Example 26, starting from(1aRS,7bSR)-5-(2-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (Intermediate 67) and 4-dimethylaminobutylamine.

¹H NMR (DMSO-d₆) δ: 13.0-12.0 (1H, br s), 7.58 (1H, dd), 7.28 (1H, dt),7.02 (2H, s), 6.69 (1H, d), 6.55 (1H, t), 5.70 (1H, m), 4.14 (1H, d),3.53 (1H, d), 3.15 (2H, m), 2.91 (2H, m), 2.67 (6H, s), 1.83 (1H, m),1.76 (2H, m), 1.66 (1H, m), 1.53 (2H, m), 0.84 (1H, m), 0.67 (1H, m).

LCMS (Method C) r/t 3.43 (M+H) 460.

Examples 30 and 31 Separation of Enantiomers from Example 29

Sample from Example 29 was subjected to chiral separation using aChiralPak IB column 20 mm×250 mm, particle size 5 micron. Elutingsolvent hexane:ethanol:diethylamine (49.8:50:0.2).

Example 30 First Eluting Enantiomer: r/t on Analytical Column (4.6mm×250 mm) 12.69 Minutes (>98% Ee)

¹H NMR (DMSO-d₆) δ: 13.0-12.2 (1H, br s), 7.58 (1H, dd), 7.28 (1H, dt),7.02 (2H, m), 6.69 (1H, d), 6.55 (1H, t), 5.71 (1H, m), 4.14 (1H, d),3.53 (1H, d), 3.15 (2H, m), 2.89 (2H, m), 2.67 (6H, s), 1.83 (1H, m),1.76 (2H, m), 1.66 (1H, m), 1.54 (2H, m), 0.85 (1H, m), 0.68 (1H, m).

LCMS (Method C) r/t 3.33 (M+H) 460.

Example 31 Second Eluting Enantiomer: r/t on Analytical Column (4.6mm×250 mm) 16.82 Minutes (>98% Ee)

¹H NMR (DMSO-d₆) δ: 12.9-12.1 (1H, br s), 7.58 (1H, dd), 7.28 (1H, dt),7.02 (2H, s), 6.70 (1H, d), 6.55 (1H, t), 5.71 (1H, m), 4.14 (1H, d),3.53 (1H, d), 3.15 (2H, m), 2.91 (2H, m), 2.68 (6H, s), 1.83 (1H, m),1.77 (2H, m), 1.66 (1H, m), 1.54 (2H, m), 0.85 (1H, m), 0.68 (1H, m).

LCMS (Method C) r/t 3.33 (M+H) 460.

Example 32(1aRS,7bSR)-5-[2-(5-Dimethylaminopentylamino)benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a similar manner to Example 26, starting from(1aRS,7bSR)-5-(2-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (Intermediate 67) and 5-dimethylaminopentylamine.

¹H NMR (DMSO-d₆) δ: 12.8-12.2(1H, br s), 7.67 (1H, dd), 7.30 (1H, dt),6.98 (1H, d), 6.85 (1H, d), 6.68 (1H, d), 6.60 (1H, t), 5.54 (1H, m),4.14 (1H, d), 3.54 (1H, d), 3.05 (4H, m), 2.66 (6H, s), 1.81 (1H, m),1.63 (5H, m), 1.51 (2H, m), 0.83 (1H, m), 0.67 (1H, m).

LCMS (Method C) r/t 3.55 (M+H) 474.

Example 33(1aRS,7bSR)-5-{2[(Z)-3-(Propan-2-yl)aminoprop-1-enyl]-4-fluorobenzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of methyl(1aRS,7bSR)-5-{2[(Z)-3-(propan-2-yl)aminoprop-1-enyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 69, 0.12 g) and lithium hydroxide monohydrate (0.1 g) in amixture of dioxane (10 mL) and water (5 mL) was stirred and heated at100° C. overnight. After cooling, the mixture was concentrated undervacuum and the residue was acidified to pH4 with formic acid thenextracted with a mixture of ethyl acetate and THF (1:1). The organicphase was dried (Na₂SO₄) and filtered. The filtrate was evaporated todryness and the residue was dissolved in ethyl acetate (2 mL) and hexanewas added (10 mL). The solid was collected by filtration and washed withether to give(1aRS,7bSR)-5-{2[(Z)-3-(propan-2-yl)aminoprop-1-enyl]-4-fluorobenzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.04 g) as an off white solid.

¹H NMR (DMSO-d₆) δ: 10.5-9.8 (1H, br s), 7.54 (1H, dd), 7.23-7.08 (3H,m), 7.04 (1H, d), 6.96 (1H, d), 5.91 (1H, m), 4.09 (1H, d), 3.63 (2H,m), 3.53 (1H, m), 3.49 (1H, d), 1.85 (1H, m), 1.67 (1H, m), 1.16 (6H,d), 0.86 (1H, m), 0.67 (1H, m).

LCMS (Method C) r/t 3.37 (M+H) 461.

Example 34(1aRS,7bSR)-5-{2[(Z)-3-((S)-3-Hydroxypyrrolidin-1-yl)aminoprop-1-enyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a similar manner to Example 33, starting frommethyl(1aRS,7bSR)-5-{2[(Z)-3-((S)-3-hydroxypyrrolidin-1-yl)aminoprop-1-enyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 70).

¹H NMR (DMSO-d₆) δ: 12.5-11.3 (1H, br s), 7.62 (1H, m), 7.32 (1H, d),7.22 (2H, m), 7.13 (1H, d), 6.98 (1H, d), 6.12 (1H, m), 5.26 (1H, m),4.37 (1H, m), 4.19 (1H, d), 3.79 (2H, m), 3.59 (1H, dd), 3.20-3.00 (3H,br s), 2.05 (1H, m), 1.94 (1H, m), 1.77 (2H, m), 0.96 (1H, m), 0.76 (1H,m).

LCMS (Method C) r/t 3.15 (M+H) 489.

Example 35(1aRS,7bSR)-5-{2[(Z)-3-((R)-3-Hydroxypyrrolidin-1-yl)aminoprop-1-enyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a similar manner to Example 33, starting frommethyl(1aRS,7bSR)-5-{2[(Z)-3-((R)-3-hydroxypyrrolidin-1-yl)aminoprop-1-enyl]-4-fluorobenzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 71).

¹H NMR (DMSO-d₆) δ: 12.5-11.4 (1H, br s), 7.62 (1H, m), 7.33 (1H, d),7.22 (2H, m), 7.13 (1H, d), 6.98 (1H, d), 6.14 (1H, m), 5.26 (1H, m),4.37 (1H, m), 4.19 (1H, d), 3.79 (2H, m), 3.59 (1H, dd), 3.20-3.00 (3H,br s), 2.05 (1H, m), 1.94 (1H, m), 1.77 (2H, m), 0.96 (1H, m), 0.76 (1H,m).

LCMS (Method C) r/t 3.14 (M+H) 489.

Example 36(1aRS,7bSR)-5-[2((Z)-4-Diethylaminobut-1-enyl)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a manner similar to Example 33, starting frommethyl(1aRS,7bSR)-5-{N-(methoxycarbonyl)-N-[2((Z)-4-diethylaminobut-1-enyl)-4-fluorobenzenesulfonyl]amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 72).

¹H NMR (DMSO-d₆) δ: 12.8-11.4 (1H, br s), 7.54 (1H, dd), 7.14-7.02 (4H,m), 6.83 (1H, d), 5.66 (1H, m), 4.09 (1H, d), 3.51 (1H, d), 3.13 (2H,m), 2.92 (4H, m), 2.34 (2H, m), 1.84 (1H, m), 1.66 (1H, m), 1.06 (6H,t), 0.86 (1H, m), 0.67 (1H, m).

LCMS (Method C) r/t 3.35 (M+H) 489.

Examples 37 and 38 Separation of Enantiomers from Example 36

Sample from Example 37 was subjected to chiral separation using aChiralPak IC column, 10 mm×250 mm, particle size 5 micron. Elutingsolvent tert-butyl methyl ether:isopropanol:DCM (16:20:64).

Example 37 First Eluting Enantiomer: r/t on Analytical Column (4.6mm×250 mm): 25.8 Minutes >98% Ee

¹H NMR (DMSO-d₆) δ: 7.61 (1H, dd), 7.20-7.09 (4H, m), 6.90 (1H, d), 5.74(1H, m), 4.16 (1H, d), 3.58 (1H, d), 3.22-3.11 (2H, m), 2.99 (4H, m),2.50 (2H, m), 1.92 (1H, dt), 1.72 (1H, m), 1.15 (6H, t), 0.93 (1H, m),0.75 (1H, m).

LCMS (Method C) r/t 3.36 (M+H) 489

Example 38 Second Eluting Enantiomer: r/t on Analytical Column 44.0Minutes, >98% Ee

¹H NMR (DMSO-d₆) δ: 7.61 (1H, dd), 7.20-7.10 (4H, m), 6.90 (1H, d), 5.74(1H, m), 4.16 (1H, d), 3.58 (1H, d), 3.23-3.10 (2H, m), 2.99 (4H, q),2.51 (2H, m), 1.92 (1H, dt), 1.72 (1H, m), 1.15 (6H, t), 0.93 (1H, m),0.75 (1H, m).

LCMS (Method C) r/t 3.36 (M+H) 489

Example 39(1aRS,7bSR)-5-{2-[2-(4-Ethylpiperazin-1-yl)-ethyl]-4-fluorobenzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A solution of(1aRS,7bSR)-5-(4-Fluoro-2-vinylbenzenesulfonylamino)-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylicacid (Intermediate 74, 0.035 g) and 3 drops of N-ethyl piperazine inisopropanol (0.5 mL) was irradiated in the microwave at 160° C. for 15minutes then again at 170° C. for 15 minutes. After cooling, the mixturewas purified by preparative HPLC (C18) eluting with a mixture ofmethanol and water, containing 0.1% formic acid, with a gradient of20-60%. The isolated product was further purified by chromatography onsilica eluting with a mixture of methanol and DCM with a gradient of0-10% to give(1aS,7bR)-5-{2-[2-(4-ethylpiperazin-1-yl)-ethyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.018 g) as an off white solid.

¹H NMR (CDCl₃) δ: 7.95 (1H, dd), 7.07 (2H, s), 6.95 (1H, dd), 6.91 (1H,dt), 4.38 (1H, d), 3.79 (1H, d), 3.42 (2H, q), 3.35 (2H, q), 3.21-3.05(4H, m), 3.04-2.88 (4H, m), 2.79 (2H, m), 1.86 (1H, dt), 1.66 (1H, m),1.22 (3H, t), 1.06 (1H, q), 0.93 (1H, m).

LCMS (Method C) r/t 2.95 (M+H) 504

Example 40(1aRS,7bSR)-5-{2[(Z)-3-(Azetidin-1-yl)prop-1-enyl]-4-fluorobenzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a manner similar to Example 33, starting frommethyl(1aRS,7bSR)-5-{2-[(Z)-3-(azetidin-1-yl)prop-1-enyl]-4-fluorobenzenesulfonyl-amino}-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate(Intermediate 76).

¹H NMR (DMSO-d₆) δ: 12.8-11.1 (1H, br s), 7.51 (1H, dd), 7.26 (1H, d),7.17 (1H, dt), 7.10 (2H, m), 7.00 (1H, d), 5.90 (1H, m), 4.12 (1H, d),3.96 (4H, m), 3.74 (2H, m), 3.52 (1H, d), 2.27 (2H, m), 1.89 (1H, m),1.69 (1H, m), 0.90 (1H, m), 0.69 (1H, m).

LCMS (Method C) r/t 3.26 (M+H) 459.

Example 41(1aRS,7bSR)-5-{2[(Z)-3-(3-Hydroxyazetidin-1-yl)prop-1-enyl]-4-fluorobenzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a manner similar to Example 33, starting frommethyl(1aRS,7bSR)-5-{2-[(Z)-3-(3-hydroxyazetidin-1-yl)prop-1-enyl]-4-fluorobenzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 77).

¹H NMR (DMSO-d₆) δ: 12.8-11.2 (1H, br s), 7.53 (1H, m), 7.22 (1H, d),7.17 (1H, dt), 7.09 (2H, m), 6.97 (1H, d), 5.90 (1H, m), 4.40 (1H, m),4.18 (2H, m), 4.12 (1H, d), 3.69 (4H, m), 3.52 (1H, d), 1.87 (1H, m),1.69 (1H, m), 0.89 (1H, m), 0.70 (1H, m).

LCMS (Method C) r/t 3.18 (M+H) 475.

Example 42(1aRS,7bSR)-5-{2[(Z)-3-(Azetidin-1-yl)propyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A solution of(1aRS,7bSR)-5-{2[(Z)-3-(azetidin-1-yl)prop-1-enyl]-4-fluorobenzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (Example 40, 0.03 g) in methanol was treated, under an atmosphereof nitrogen with palladium on carbon (10%, 0.01 g). The nitrogen wasreplaced by hydrogen and the mixture was stirred under an atmosphere ofhydrogen overnight. The mixture was filtered and the filtrate wasevaporated to dryness. The residue was purified by HPLC (C18) to give(1aRS,7bSR)-5-{2[(Z)-3-(azetidin-1-yl)propyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.019 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.76 (1H, dd), 7.20 (1H, dd), 7.09 (1H, dt), 7.05(1H, d), 6.99 (1H, d) 4.15 (1H, d), 3.97 (2H, m) 3.56 (1H, d), 3.14 (2H,m), 2.99 (4H, m), 2.29 (2H, m), 1.86 (1H, m), 1.81-1.64 (3H, m), 0.88(1H, m), 0.69 (1H, m).

¹H LCMS (Method C) r/t 3.20 (M+H) 461.

Example 43(1aRS,7bSR)-5-[2((Z)-4-Diethylaminobutyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a similar manner to Example 42, starting from(1aRS,7bSR)-5-[2((Z)-4-diethylaminobut-1-enyl)-4-fluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid (Example 36) as a white solid.

¹H NMR (DMSO-d₆) δ: 13.0-11.6 (1H, br s), 7.82 (1H, dd), 7.21 (1H, dd),7.08 (1H, dt), 7.02 (1H, d), 6.96 (1H, d), 4.14 (1H, d), 3.55 (1H, d),2.99 (8H, m), 1.83 (1H, m), 1.65 (5H, m), 1.14 (6H, t), 0.85 (1H, m),0.69 (1H, m).

LCMS (Method C) r/t 3.45 (M+H) 491.

Example 44(1aRS,7bSR)-5-{2-[N-(4-Dimethylaminobutyl)-N-methylamino]-benzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of(1aRS,7bSR)-5-(2-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid (Intermediate 67, 0.1 g), N-(4-dimethylaminobutyl)-N-methylamine(Intermediate 78, 1.07 g) and triethylamine (0.42 g) in NMP (6 mL) wasstirred and heated in a sealed tube at 150° C. for 3 days. Aftercooling, the mixture was concentrated under vacuum and the residue waspurified by chromatography on silica, eluting with a mixture of methanoland DCM (10%) followed by repurification by HPLC (C18) to give(1aRS,7bSR)-5-{2-[N-(4-dimethylaminobutyl)-N-methylamino]-benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.03 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.81 (1H, dd), 7.54 (1H, dt), 7.41 (1H, dd), 7.21(1H, dt), 6.94 (1H, d), 6.85 (1H, d), 4.12 (1H, d), 3.55 (1H, d), 2.96(2H, t), 2.85 (2H, t), 2.64 (6H, s), 2.49 (3H, s), 1.83 (1H, m), 1.74(2H, m), 1.63 (3H, m), 0.87 (1H, m), 0.68 (1H, m).

LCMS (Method C) r/t 3.37 (M+H) 474.

Example 45(1aRS,7bSR)-5-{2-[((S)-1-Ethylpyrrolidin-3-ylcarbamoyl)methyl]-4-fluoro-benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of methyl(1aRS,7bSR)-5-{2-[((S)-1-ethylpyrrolidin-3-ylcarbamoyl)methyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 80, 0.148 g) and lithium hydroxide monohydrate (0.168 g)in dioxane (3 mL) and water (1 mL) was irradiated in the microwave at130° C. for 40 minutes. After cooling, the mixture was diluted withmethanol, acidified with formic acid and evaporated in vacuo. Theresidue was triturated with 10% methanol in DCM and filtered. Thefiltrate was evaporated in vacuo and the residue was purified bychromatography on silica, eluting with a mixture of methanol and DCMwith a gradient of 0-20%. The resultant solid was triturated with etherand filtered off to give(1aRS,7bSR)-5-{2-[((S)-1-ethylpyrrolidin-3-ylcarbamoyl)methyl]-4-fluorobenzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.091 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 9.56 (0.5H, br, d), 9.48 (0.5H, br, d), 7.59 (1H,m), 7.34 (1H, m), 7.16 (2H, m), 7.06 (1H, t), 4.46 (1H, br, q), 4.13(1H, d), 3.92 (1H, dd), 3.70 (1H, m), 3.65 (1H, d), 3.58 (1H, br, m),2.95-3.25 (6H, m), 2.40 (1H, m), 1.95 (2H, m), 1.76 (1H, m), 1.20 (3H,t), 0.97 (1H, m), 0.78 (1H, m).

LCMS (Method C) r/t 3.04 (M+H) 518.

Example 46(1aRS,7bSR)-5-[2-(1-Ethylazetidin-3-yl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a similar manner to Example 45, starting frommethyl(1aRS,7bSR)-5-[2-(1-ethylazetidin-3-yl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(Intermediate 86) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.91 (1H, dd), 7.64 (1H, dd), 7.24 (1H, dt), 6.96(1H, d), 6.66 (1H, d), 4.79 (1H, m), 4.21 (1H, d), 4.15 (2H, br, t),3.89 (2H, br, m), 3.62 (1H, d), 3.06 (2H, q), 1.83 (1H, m), 1.70 (1H,m), 1.05 (3H, t), 0.88 (1H, m), 0.72 (1H, m).

LCMS (Method C) r/t 2.99 (M+H) 447.

Example 47(1aRS,7bSR)-5-{2-[((R)-1-Ethylpyrrolidin-3-ylcarbamoyl)methyl]-4-fluoro-benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a similar manner to Example 45, starting frommethyl(1aRS,7bSR)-5-{2-[((R)-1-ethylpyrrolidin-3-ylcarbamoyl)methyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 92) as a white solid.

¹H NMR (CDCl₃) δ: 10.30 (0.5H, br, s), 10.25 (0.5H, br, s), 9.88 (1H,br, s), 7.52 (1H, m), 7.18-7.41 (3H, m), 6.75 (1H, m), 4.83 (0.5H, m),4.70 (0.5H, m), 4.17 (1.5H, m), 3.84-4.10 (1.5H, m), 3.60-3.86 (3H, m),3.45 (0.5H, d), 3.31 (0.5H, m), 3.13 (0.5H, m), 2.98 (0.5H, m), 2.83(2H, m), 2.46 (1H, m), 2.29 (1H, m), 1.93 (1H, m), 1.67 (1H, q), 1.40(3H, t), 1.13 (0.5H, m), 1.07 (0.5H, m), 0.97 (1H, m).

LCMS (Method C) r/t 3.03 (M+H) 518.

Example 48(1aRS,7bSR)-5-{2-[2-(Pyrrolidin-1-yl)-ethyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a similar manner to Example 39, starting from(1aRS,7bSR)-5-(4-fluoro-2-vinylbenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (Intermediate 74) and pyrrolidine as a white solid.

¹H NMR (DMSO-d₆) δ: 7.84 (1H, dd), 7.26 (1H, dd), 7.17 (1H, dt), 7.02(1H, d), 6.74 (1H, d), 4.16 (1H, d), 3.59 (1H, d), 3.36-3.20 (8H, m),1.91 (4H, m), 1.85 (1H, m), 1.69 (1H, m), 0.89 (1H, m), 0.70 (1H, m).

LCMS (Method C) r/t 3.12 (M+H) 461.

Example 49(1aRS,7bSR)-5-[2-((R)-1-Ethylpyrrolidin-3-ylmethyl)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Lithium hydroxide (0.11 g) was added to a solution of methyl(1aRS,7bSR)-5-[2-((R)-1-ethyl-pyrrolidin-3-ylmethyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(Intermediate 95, 0.13 g) in a mixture of dioxane (4 mL) and water (1mL) and the mixture was stirred and heated at 85° C. overnight. Aftercooling, the mixture was filtered and the filtrate was acidified byaddition of 10% aqueous citric acid (1 mL) and then extracted with DCM.The organic extract was dried (MgSO₄) and filtered. The filtrate wasevaporated to dryness and the residue was triturated with diethyl etherand the solid was collected by filtration to give(1aRS,7bSR)-5-[2-((R)-1-ethylpyrrolidin-3-ylmethyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.085 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.81 (1H, dd), 7.28 (1H, dd), 7.16 (1H, dt), 7.11(1H, dd), 6.99 (1H, dd), 4.20 (1H, dd), 3.60 (1H, t), 3.48-2.98 (9H, brm), 2.25 (1H, m), 1.91 (1H, dt), 1.73 (2H, m), 1.23 (3H, t), 0.93 (1H,dt), 0.75 (1H, m).

LCMS (Method C) r/t 3.21 (M+H) 475.

Examples 50 and 51 Separation of Enantiomers from Example 49

Sample from Example 49 was subjected to chiral separation using aChiralPak IC column, 10 mm×250 mm, particle size 5 micron. Elutingsolvent tert-butyl methyl ether:isopropanol:DCM (10:15:75).

Example 50 First Eluting Enantiomer: r/t on Analytical Column (4.6mm×250 mm): 30.0 Minutes >99% Ee

¹H NMR (DMSO-d₆) δ: 7.81 (1H, dd), 7.27 (1H, dd), 7.15 (1H, dt), 7.10(1H, d), 7.01 (1H, d), 4.20 (1H, d), 3.58 (1H, d), 3.23-3.11 (6H, m),3.11-3.06 (3H, m), 2.25 (1H, m), 1.91 (1H, dt), 1.73 (2H, m), 1.22 (3H,t), 0.92 (1H, dt), 0.73 (1H, m).

LCMS (Method C) r/t 3.25 (M+H) 475.

Example 51 Second Eluting Enantiomer: r/t on Analytical Column 40.0Minutes, >99% Ee

¹H NMR (DMSO-d₆) δ: 7.80 (1H, dd), 7.27 (1H, dd), 7.15 (1H, dt), 7.10(1H, d), 7.03 (1H, d), 4.18 (1H, d), 3.61 (1H, d), 3.48-2.97 (9H, br m),2.27 (1H, m), 1.91 (1H, dt), 1.71 (2H, m), 1.23 (3H, t), 0.93 (1H, dt),0.74 (1H, m).

LCMS (Method C) r/t 3.23 (M+H) 475.

Example 52(1aRS,7bSR)-5-{2-[((S)-1-Ethylpyrrolidin-2-yl)cabonylaminomethyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of methyl(1aRS,7bSR)-5-{2-[((S)-1-ethylpyrrolidin-2-yl)cabonylaminomethyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(Intermediate 101, 0.212 g) and lithium hydroxide (0.05 g) in dioxane(5.5 mL) and water (2.5 mL) was irradiated in the microwave at 150° C.for 30 minutes. After cooling, the mixture was diluted with water,acidified with formic acid to pH5 and extracted with ethyl acetate. Theorganic layer was washed with water, dried (MgSO₄) and filtered. Thefiltrate was evaporate to dryness and the residue was purified by HPLC(C18) eluting with a mixture of methanol and water, containing 0.1%formic acid, with a gradient of 35-75% to give(1aRS,7bSR)-5-{2-[((S)-1-ethylpyrrolidin-2-yl)cabonylaminomethyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid (0.064 g) as a white solid.

¹H NMR (CDCl₃) δ: 10.8-9.6 (1H, br s), 8.90 (1H, br t), 7.71 (1H, m),7.20 (3H, m), 6.86 (1H, m), 4.88 (2H, m), 4.37 (1H, dd), 3.85 (1H, dt),3.61 (1H, m), 3.43 (1H, m), 2.97 (1H, m), 2.77 (2H, m), 2.23 (2H, m),2.03 (1H, m), 1.91 (2H, m), 1.69 (1H, m), 1.18 (3H, q), 1.01 (2H, m).

LCMS (Method C) r/t 3.09 (M+H) 518.

Example 53(1aRS,7bSR)-5-[2-(4-Dimethylaminobutyrylamino)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of methyl(1aRS,7bSR)-5-[2-(4-dimethylaminobutyryl)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 108, 0.2 g), potassium carbonate (0.22 g),1H-pyrazole-3-amine (0.34 g) and lithium iodide (1.07 g) in DMF (10 mL)was irradiated in the microwave at 150° C. for 1 hour. After cooling,the mixture was diluted with methanol and acidified to pH 3 with formicacid then concentrated under vacuum. The residue was purified bychromatography on silica, eluting with a mixture of methanol and DCM(5%). The resultant product was purified by HPLC (C18) to give(1aRS,7bSR)-5-[2-(3-dimethylaminobutyryl)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid (0.03 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.95 (1H, dd), 7.80 (1H, dd), 6.96 (1H, d), 6.95(1H, dt), 6.79 (1H, d), 4.13 (1H, d), 3.56 (1H, d), 3.04 (2H, t), 2.68(6H, s), 2.56 (2H, t), 1.94 (2H, m), 1.81 (1H, m), 1.64 (1H, m), 0.84(1H, m), 0.66 (1H, m).

LCMS (Method C) r/t 3.12 (M+H) 492.

Example 54(1aRS,7bSR)-5-[2-((S)-1-Ethylpyrrolidin-3-ylmethyl)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a similar manner to Example 49, starting frommethyl(1aRS,7bSR)-5-[2-((S)-1-ethylpyrrolidin-3-ylmethyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate(Intermediate 113).

¹H NMR (DMSO-d₆) δ: 7.81 (1H, dd), 7.27 (1H, dd), 7.15 (1H, dt), 7.10(1H, d), 7.02 (1H, dd), 4.19 (1H, dd), 3.56 (1H, t), 3.23-3.11 (6H, m),3.11-3.06 (3H, m), 2.25 (1H, m), 1.91 (1H, dt), 173 (2H, m), 1.22 (3H,t), 0.92 (1H, dt), 0.73 (1H, m).

LCMS (Method C) r/t 3.21 (M+H) 475.

Example 55(1aRS,7bSR)-5-[2-(3-Dimethylaminopropylcarbamoyl)benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid

A solution of tert-butyl(1aRS,7bSR)-5-{2-[N-(2,4-dimethoxybenzyl)-N-(3-dimethylamino-propyl)carbamoyl]benzenesulfonylamino}-1,1a,2,7b-tetrahydro-cyclopropa-[c]chromene-4-carboxylate(Intermediate 119, 0.03 g) in trifluoroacetic acid (5 mL) was stirredand heated at 30° C. overnight. The mixture was evaporated to drynessand the residue was purified by HPLC (C18) to give(1aRS,7bSR)-5-[2-(3-dimethylaminopropylcarbamoyl)benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.013 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 8.61 (1H, br t), 7.73 (1H, d), 7.52 (1H, t), 7.43(2H, m), 6.97 (1H, d), 6.82 (1H, d), 4.14 (1H, d), 3.58 (1H, d), 3.26(2H, m), 3.04 (2H, t), 2.60 (6H, s), 1.85 (3H, m), 1.67 (1H, m), 0.87(1H, m), 0.68 (1H, m).

LCMS (Method C) r/t 2.79 (M+H) 473.

Example 56(1aRS,7bSR)-5-(2-{[N—((S)-1-Ethylpyrrolidin-3-yl)-N-methylcarbamoyl]methyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of methyl(1aRS,7bSR)-5-(2-{[N—((S)-1-ethylpyrrolidin-3-yl)-N-methylcarbamoyl]-methyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 126, 0.047 g) and lithium hydroxide monohydrate (0.168 g)in dioxane (3 mL) and water (1 mL) was irradiated in the microwave at130° C. for 40 minutes. After cooling, the mixture was diluted withmethanol, acidified with formic acid and evaporated in vacuo. Theresidue was triturated with 10% methanol in DCM, filtered and thefiltrate was evaporated in vacuo. The residue was purified bychromatography on silica, eluting with a mixture of methanol and DCMwith a gradient of 0-40%. The resultant solid was triturated with ethylacetate and filtered off to give(1aRS,7bSR)-5-(2-{[N—((S)-1-ethylpyrrolidin-3-yl)-N-methylcarbamoyl]-methyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.022 g) as a white solid.

¹H NMR (DMSO-d₆ at 80° C.) δ: 7.83 (1H, t), 7.12 (1H, dt), 7.08 (1H, d),7.01 (1H, d), 6.84 (1H, m), 4.61 (1H, br, s), 4.19 (1H, d), 4.12 (2H,s), 3.73 (1H, d), 2.71-3.18 (7H, br, m), 2.94 (3H, s), 1.85-2.15 (3H,m), 1.72 (1H, m), 1.17 (3H, t), 0.95 (1H, m), 0.78 (1H, m).

LCMS (Method C) r/t 3.08 (M+H) 532.

Example 57(1aRS,7bSR)-5-(2-{[N—((R)-1-Ethylpyrrolidin-3-yl)-N-methylcarbamoyl]methyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of methyl(1aRS,7bSR)-5-(2-{[N—((R)-1-ethylpyrrolidin-3-yl)methylcarbamoyl]-N-methyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 131, 0.076 g) and lithium hydroxide monohydrate (0.168 g)in dioxane (3 mL) and water (1 mL) was irradiated in the microwave at130° C. for 40 minutes. After cooling the mixture was diluted withmethanol, acidified with formic acid and evaporated in vacuo. Theresidue was triturated with 10% methanol in DCM, filtered and thefiltrate was evaporated in vacuo. The residue was purified bychromatography on silica, eluting with a mixture of methanol and DCMwith a gradient of 0-40%. The resultant solid was triturated with ethylacetate and filtered off to give(1aRS,7bSR)-5-(2-{[N—((R)-1-ethylpyrrolidin-3-yl)-N-methylcarbamoyl]-methyl}-4-fluoro-benzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.028 g) as a white solid.

¹H NMR (DMSO-d₆ at 80° C.) δ: 7.83 (1H, t), 7.12 (1H, dt), 7.08 (1H, d),7.01 (1H, d), 6.84 (1H, m), 4.61 (1H, br, s), 4.19 (1H, d), 4.12 (2H,s), 3.73 (1H, d), 2.71-3.18 (7H, br, m), 2.94 (3H, s), 1.85-2.15 (3H,m), 1.72 (1H, m), 1.17 (3H, t), 0.95 (1H, m), 0.78 (1H, m).

LCMS (Method C) r/t 3.08 (M+H) 532.

Example 58(1aRS,7bSR)-5-{2-[2-((S)-1-Ethylpyrrolidin-2-yl)ethylamino]benzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of(1aRS,7bSR)-5-(2-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid (Intermediate 67, 0.1 g), 2-((S)-1-ethylpyrrolidin-2-yl)ethylamine(Intermediate 136, 0.5 g) and triethylamine (0.5 mL) was stirred andheated in a sealed tube at 140° C. overnight. After cooling, the mixturewas concentrated under vacuum and the residue was purified bychromatography on silica, eluting with a mixture of methanol and DCM(10%). The product was repurified by HPLC (C18) to give(1aRS,7bSR)-5-{2-[2-((S)-1-ethylpyrrolidin-2-yl)ethylamino]benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.022 g) as a white solid.

NMR (DMSO-d₆) δ: 7.47 (1H, m), 7.25 (1H, t), 6.92 (1H, d), 6.89 (1H, m),6.72 (1H, d), 6.53 (1H, dt),6.0-5.3 (1H, br s), 4.11 (1H, dd), 3.53 (1H,t), 3.33-2.80 (7H, m), 2.19 (2H, m), 1.92 (2H, m), 1.82 (2H, m), 1.64(2H, m), 1.17 (3H, t), 0.84 (1H, m), 0.67 (1H, m).

LCMS (Method C) r/t 3.34 (M+H) 486.

Example 59(1aRS,7bSR)-5-{2-[2-((R)-1-Ethylpyrrolidin-2-yl)ethylamino]benzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a similar manner to Example 58, starting from(1aRS,7bSR)-5-(2-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid (Intermediate 67) and 2-((R)-1-ethylpyrrolidin-2-yl)ethylamine(Intermediate 141).

¹H NMR (DMSO-d₆) δ: 7.47 (1H, m), 7.25 (1H, t), 6.97 (1H, d), 6.90 (1H,m), 6.72 (1H, d), 6.53 (1H, dt), 6.0-5.4 (1H, br s), 4.12 (1H, dd), 3.53(1H, t), 3.35-2.85 (7H, m), 2.20 (2H, m), 1.93 (2H, m), 1.81 (2H, m),1.65 (2H, m), 1.18 (3H, t), 0.84 (1H, m), 0.67 (1H, m).

LCMS (Method C) r/t 3.32 (M+H) 486.

Example 60(1aRS,7bSR)-5-[2-(3-N,N,-Diethylaminopropylamino)benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

3-Diethylaminopropyl amine (0.975 g) was added to a solution of(1aRS,7bSR)-5-(2-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (Intermediate 67, 0.091 g) in NMP (3 mL) and the mixture was heatedat 140° C. in a sealed tube for 36 hours. After cooling, the mixture wasdiluted with water (2 mL) and the solution was purified by preparativeHPLC (C18) eluting with a mixture of methanol and water, containing 0.1%formic acid, with a gradient of 10-98% to give(1aRS,7bSR)-5-[2-(3-diethylaminopropylamino)benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.039 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.45 (1H, dd), 7.28 (1H, dt), 7.04 (2H, m), 6.74(1H, d), 6.51 (1H, t), 6.17 (1H, br s), 4.16 (1H, d), 3.57 (1H, d),3.54-2.97 (8H, br m), 1.87 (1H, dt), 1.81-1.63 (3H, m), 1.15 (6H, t),0.89 (1H, m), 0.72 (1H, m).

LCMS (Method C) r/t 3.31 (M+H) 474.

Example 61(1aRS,7bSR)-5-(2-{[((R)-1-Ethylpyrrolidine-2-yl)carbonylamino]methyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of methyl(1aRS,7bSR)-5-(2-{[((R)-1-ethylpyrrolidine-2-yl)carbonylamino]methyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 146, 0.120 g) and lithium hydroxide monohydrate (0.095 g)was suspended in dioxane (5 mL) and water (1 mL) and the mixture wasstirred and heated at 110° C. for 22.5 hours. After cooling, thevolatiles were removed in vacuo and the residue was acidified byaddition of aqueous citric acid solution (10%) and extracted with DCM.The organic layer was dried (Na₂SO₄) and filtered and the filtrate wasevaporated to dryness. The residue was purified by preparative HPLC(C18) eluting with a mixture of methanol and water, containing 0.1%formic acid, with a gradient of 10-98% to give(1aRS,7bSR)-5-(2-{[((R)-1-ethylpyrrolidine-2-yl)carbonylamino]methyl)}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid (0.043 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 8.77 (1H, d), 7.83 (1H, dd), 7.22 (1H, td), 7.12(1H, dd), 7.08 (1H, d), 6.16 (1H, dd), 4.73 (2H, d), 4.24 (1H, d), 3.67(1H, d), 3.54 (1H, br s), 3.37-3.28 (1H, m), 2.93-2.80 (1H, m),2.80-2.61 (2H, m), 2.30-2.20 (1H, m), 1.95-1.70 (5H, m), 1.08 (3H, t),0.95 (1H, dt), 0.76 (1H, q).

LCMS (Method C) r/t 3.09 (M+H) 518.

Example 62(1aRS,7bSR)-5-{2-[(1-Ethylazetidin-3-ylmethyl)amino]benzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of(1aRS,7bSR)-5-(2-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic(Intermediate 67, 0.07 g) and (1-ethylazetidin-3-yl)methylamine(Intermediate 149, 0.7 g) in DMSO (1.4 mL) was divided evenly between 7microwave vials and each was irradiated in the microwave at 130° C. for4 hours. After cooling, the combined mixture was concentrated undervacuum and the residue was purified by chromatography on silica, elutingwith a mixture of methanol and DCM (10%). The product was repurified byHPLC (C18) to give(1aRS,7bSR)-5-{2-[(1-ethylazetidin-3-ylmethyl)amino]benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.012 g) as an off-white solid.

¹H NMR (DMSO-d₆) δ: 7.34 (1H, d), 7.22 (1H, t), 7.04 (1H, d), 6.97 (1H,d), 6.74 (1H, d), 6.49 (1H, t), 6.34 (1H, br s), 4.10 (1H, d), 3.75-3.55(4H, m), 3.18 (1H, br m), 3.03 (1H, br m), 2.88 (2H, m), 2.32 (1H, m),1.85 (1H, m), 1.67 (1H, m), 1.19 (1H, m), 0.98 (3H, t), 0.86 (1H, m),0.69 (1H, m)

LCMS (Method C) r/t 3.21 (M+H) 457.

Examples 63 and 64(1aR,7bS)-5-[2-((Z)-3-Diethylaminoprop-1-enyl)benzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid and(1aS,7bR)-5-[2-((Z)-3-diethylaminoprop-1-enyl)benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid

A mixture of methyl(1aRS,7bSR)-5-[2-((Z)-3-diethylaminoprop-1-enyl)benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 153, 0.495 g) and lithium hydroxide monohydrate (0.442 g)was suspended in dioxane (20 mL) and water (5 mL) and the mixture wasstirred and heated at 80° C. for 12.5 hours. After cooling, thevolatiles were removed in vacuo and the residue was acidified byaddition of aqueous citric acid solution (10%) and extracted with DCM.The organic layer was dried (Na₂SO₄) and filtered. The filtrate wasevaporated to dryness and the residue was purified by preparative HPLC(C18) eluting with a mixture of acetonitrile and water, containing 0.1%formic acid, with a gradient of 35-70% to give(1aRS,7bSR)-5-[2-((Z)-3-diethylaminoprop-1-enyl)benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.147 g) as a white solid.

This material was subjected to chiral separation using a ChiralPak ICcolumn, 4.6 mm×250 mm, particle size 5 micron. Eluting solvent absoluteethanol,

Example 63 First Eluting Enantiomer: Retention Time on Above Column:25.71 Minutes, >99% Ee

¹H NMR (DMSO-d₆) δ: 7.65 (1H, dd), 7.60 (1H, td), 7.44-7.37 (2H, m),7.28 (1H, d), 7.08 (1H, d), 6.95 (1H, d), 6.15-6.05 (1H, m), 4.16 (1H,d), 3.77-3.67 (2H, m), 3.56 (1H, d), 3.13-3.03 (4H, m), 1.90 (1H, dt),1.71 (1H, q), 1.12 (6H, t), 0.92 (1H, dt), 0.72 (1H, q).

LCMS (Method C) r/t 3.20 (M+H) 457.

Example 64 Second Eluting Enantiomer: Retention Time on Above Column35.51 Minutes, >99% Ee

¹H NMR (DMSO-d₆) δ: 7.65 (1H, dd), 7.60 (1H, td), 7.43-7.38 (2H, m),7.28 (1H, d), 7.08 (1H, d), 6.95 (1H, d), 6.16-6.07 (1H, m), 4.16 (1H,d), 3.77-3.67 (2H, m), 3.56 (1H, d), 3.09 (4H, q), 1.91 (1H, dt), 1.71(1H, q), 1.12 (6H, t), 0.93 (1H, dt), 0.72 (1H, q).

LCMS (Method C) r/t 3.20 (M+H) 457.

Example 65(1aRS,7bSR)-5-(2-{N—[((R)-1-Ethylpyrrolidine-2-yl)carbonyl]-N-methylaminomethyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of methyl(1aRS,7bSR)-5-(2-{N—[((R)-1-ethylpyrrolidine-2-yl)carbonyl]-N-methyl-aminomethyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 155, 0.177 g) and lithium hydroxide monohydrate (0.136 g)in dioxane (5 mL) and water (2 mL) was stirred and heated at 100° C. for19.5 hours. After cooling, the mixture was evaporated to dryness and theresidue was acidified by addition of aqueous citric acid solution (10%).The resultant solid was collected by filtration, washed with water anddried under vacuum at 40° C. The solid was purified by preparative HPLC(C18) eluting with a mixture of methanol and water, containing 0.1%formic acid, with a gradient of 10-98% to give(1aRS,7bSR)-5-(2-{N—[((R)-1-ethylpyrrolidine-2-yl)carbonyl]-N-methylaminomethyl}-4-fluoro-benzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.053 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.93-7.78 (1H, m), 7.17 (1H, m), 6.99 (0.5H, m),6.95 (0.5H, d), 6.90-6.76 (1.5H, m), 6.69 (0.5H, dd), 5.02 (1.5H, m),4.86 (0.5H, dd), 4.61-4.44 (1H, br s), 4.15 (1H, dd), 3.55 (3H, m), 3.11(2H, m), 2.90 (3H, 2s), 2.06-1.54 (6H, m), 1.18-1.05 (4H, m), 0.84 (1H,m), 0.68 (1H, m).

LCMS (Method C) r/t 3.14 (M+H) 532.

Example 66(1aRS,7bSR)-5-(2-{N—[((S)-1-Ethylpyrrolidine-2-yl)carbonyl]-N-methylaminomethyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a similar manner to Example 65, starting frommethyl(1aRS,7bSR)-5-(2-{N—[((S)-1-ethylpyrrolidine-2-yl)carbonyl]-N-methylaminomethyl}-4-fluorobenzene-sulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 160) as a white solid.

¹H NMR (DMSO-d₆) 7.94-7.76 (1H, m), 7.18 (1H, m), 7.02-6.92 (1H, m),6.92-6.76 (1.5H, m), 6.68 (0.5H, m), 5.02 (1.5H, m), 4.86 (0.5H, dd),4.65-4.49 (1H, br s), 4.15 (1H, dd), 3.55 (3H, m), 3.14 (2H, m), 2.91(3H, 2s), 2.07-1.59 (6H, m), 1.13 (4H, m), 0.85 (1H, m), 0.68 (1H, m).

LCMS (Method C) r/t 3.15 (M+H) 532.

Example 67(1aRS,7bSR)-5-[2-(4-Dimethylaminobutylamino)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of methyl(1aRS,7bSR)-5-[2-(4-dimethylaminobutylamino)-4-fluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 161, 0.485 g) and lithium hydroxide monohydrate (0.505 g)in dioxane (9 mL) and water (3 mL) was irradiated in the microwave at130° C. for 45 minutes. After cooling, the mixture was diluted withmethanol, acidified with formic acid and evaporated in vacuo. Theresidue was triturated with 20% methanol in DCM, filtered and thefiltrate was evaporated in vacuo. The residue was purified bychromatography on silica, eluting with a mixture of methanol and DCMwith a gradient of 0-20%. The resultant solid was triturated with ethylacetate and filtered off to give(1aRS,7bSR)-5-[2-(4-dimethylaminobutylamino)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid (0.215 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 12.52 (2H, br, s), 7.65 (1H, dd), 7.08 (2H, q), 6.56(1H, dd), 6.39 (1H, dt), 5.98 (1H, m), 4.20 (1H, d), 3.59 (1H, d), 3.22(2H, q), 2.98 (2H, m), 2.75 (6H, s), 1.91 (1H, m), 1.81 (2H, m), 1.72(1H, m), 1.58 (2H, m), 0.92 (1H, m), 0.76 (1H, m).

LCMS (Method C) r/t 3.43 (M+H) 478.

Example 68(1aRS,7bSR)-5-{2-[((R)-1-Ethylpyrrolidin-3-ylmethyl)amino]benzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A solution of(1aRS,7bSR)-5-(2-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid (Intermediate 67, 0.105 g),((R)-1-ethylpyrrolidin-3-yl)methyl-amine (Intermediate 163, 0.5 g) andtriethylamine (0.5 g) in DMSO (1 mL) was stirred and heated at 140° C.overnight. After cooling, the mixture was concentrated under vacuum andthe residue was purified by chromatography on silica, eluting with amixture of methanol and DCM (5%). The product was purified by HPLC (C18)to give(1aRS,7bSR)-5-{2-[((R)-1-ethylpyrrolidin-3-ylmethyl)amino]benzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]-chromene-4-carboxylicacid (0.03 g) as a white solid,

¹H NMR (DMSO-d₆) δ: 7.38 (1H, dd), 7.24 (1H, t), 7.06 (2H, s), 6.81 (1H,d), 6.49 (1H, t), 6.14 (1H, br s), 4.13 (1H, dd), 3.54 (2H, m), 3.25(2H, m) 3.07 (4H, m), 2.82 (1H, m), 2.63 (1H, m), 1.96 (1H, m), 1.86(1H, m), 1.71-1.46 (2H, m), 1.19 (3H, m), 0.87 (1H, m), 0.70 (1H, m).

LCMS (Method C) r/t 3.31 (M+H) 472.

Example 69(1aRS,7bSR)-5-{2-[((S)-1-Ethylpyrrolidin-3-ylmethyl)amino]benzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A solution of(1aRS,7bSR)-5-(2-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic(Intermediate 67, 0.08 g), and ((S)-1-ethylpyrrolidin-3-yl)methylamine(Intermediate 169, 0.8 g) in DMSO (0.2 mL) was stirred and heated at120° C. for 24 hours. After cooling, the mixture was diluted withmethanol and concentrated under vacuum. The residue was purified by HPLC(C18) to give(1aRS,7bSR)-5-{2-[((S)-1-ethylpyrrolidin-3-ylmethyl)amino]benzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]-chromene-4-carboxylicacid (0.03 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.37 (1H, dd), 7.24 (1H, t), 7.05 (2H, s), 6.80 (1H,d), 6.48 (1H, t), 6.13 (1H, br s), 4.13 (1H, dd), 3.54 (2H, m), 3.24(2H, m), 3.05 (4H, m), 2.82 (1H, m), 2.62 (1H, m), 1.95 (1H, m), 1.85(1H, m), 1.71-1.46 (2H, m), 1.18 (3H, m), 0.86 (1H, m), 0.69 (1H, m).

LCMS (Method C) r/t 3.25 (M+H) 472.

Example 70(1aRS,7bSR)-5-[2-(4-Ethyl-2-oxopiperazin-1-ylmethyl)-4-fluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of methyl(1aRS,7bSR)-5-[2-(4-ethyl-2-oxopiperazin-1-ylmethyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopa[c]chromene-4-carboxylate(Intermediate 173, 0.28 g) and lithium hydroxide monohydrate (0.126 g)in dioxane (9 mL) and water (3 mL) was irradiated in the microwave at130° C. for 30 minutes. After cooling, the mixture was diluted withmethanol, acidified with formic acid and evaporated in vacuo. Theresidue was triturated with 20% methanol in DCM, filtered and thefiltrate was evaporated in vacuo. The residue was purified bychromatography on silica, eluting with a mixture of methanol and DCMwith a gradient of 0-20%. The resultant solid was triturated with etherand filtered to give(1aRS,7bSR)-5-[2-(4-ethyl-2-oxo-piperazin-1-ylmethyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid (0.176 g) as a white solid.

¹H NMR (CDCl₃) δ: 11.28 (1H, br, s), 8.02 (1H, dd), 7.31 (1H, d), 7.23(1H, d), 6.98 (2H, m), 4.98 (2H, q), 4.57 (1H, d), 4.04 (1H, d), 3.36(2H, t), 3.30 (2H, s), 2.72 (2H, t), 2.51 (2H, q), 1.96 (1H, m), 1.80(1H, m), 1.11 (4H, m), 1.03 (1H, m).

LCMS (Method C) r/t 2.96 (M+H) 504.

Example 71(1aRS,7bSR)-5-[2-(1-Ethylpiperidin-4-ylmethyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Methyl(1aRS,7bSR)-5-[2-(1-ethylpiperidin-4-ylmethyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 177, 0.279 g) and lithium hydroxide monohydrate (0.233 g)were suspended in dioxane (7 mL) and water (3 mL) and the mixture wasstirred and heated at 80° C. for 25 hours. Further lithium hydroxidemonohydrate (0.116 g) was added and the mixture heating was continuedfor 18 hours. After cooling, the volatiles were removed in vacuo, theresidue was acidified by addition of aqueous citric acid solution (10%)and saturated with sodium chloride. The mixture was extracted with DCMand the organic layer was dried (Na₂SO₄) and filtered. The filtrate wasevaporated to dryness and the residue was purified by preparative HPLC(C18), eluting with a mixture of methanol and water, containing 0.1%formic acid, with a gradient of 10-98% to give(1aRS,7bSR)-5-[2-(1-ethylpiperidin-4-ylmethyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.117 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.99 (1H, dd), 7.22-7.14 (2H, m), 6.99 (1H, d), 6.76(1H, d), 4.20 (1H, d), 3.60 (1H, d), 3.34 (2H, d), 3.02-2.88 (4H, m),2.71 (2H, br s), 1.99 (1H, br s), 1.84 (1H, dt), 1.74-1.62 (3H, m),1.56-1.40 (2H, m), 1.18 (3H, t), 0.89 (1H, dt), 0.73 (1H, q).

LCMS (Method C) r/t 3.22 (M+H) 489.

Example 72(1aRS,7bSR)-5-{2-[2-(1-Ethylazetidin-3-yl)ethyl]-4-fluorobenzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of methyl(1aRS,7bSR)-5-{2-[2-(1-ethylazetidin-3-yl)ethyl]-4-fluorobenzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(intermediate 183, 0.306 g) and lithium hydroxide monohydrate (0.421 g)in dioxane (7.5 mL) and water (2.5 mL) was irradiated in the microwaveat 130° C. for 45 minutes. After cooling, the mixture was diluted withmethanol, acidified with formic acid and evaporated in vacuo. Theresidue was triturated with 20% methanol in DCM, filtered and thefiltrate was evaporated in vacuo. The residue was purified bychromatography on silica, eluting with a mixture of methanol and DCMwith a gradient of 0-30%. The resultant solid was triturated with etherand filtered to give(1aRS,7bSR)-5-{2-[2-(1-ethyl-azetidin-3-yl)ethyl]-4-fluorbenzenesulfonylamino}1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.241 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.92 (1H, br, s), 7.35 (1H, dd), 7.22 (1H, dt), 7.17(1H, d), 6.78 (1H, br, s), 4.27 (1H, d), 4.05 (2H, m), 3.78 (2H, br, s),3.70 (1H, d), 3.17 (2H, q), 2.86 (2H, br, s), 2.70 (1H, br, s), 1.95(1H, m), 1.84 (2H, m), 1.75 (1H, m), 1.11 (3H, t), 0.98 (1H, m), 0.76(1H, m).

LCMS (Method C) r/t 3.36 (M+H) 475.

Example 73(1aRS,7bSR)-5-{2-[((S)-1-Azabicyclo[2.2.2]oct-3-yl)amino]benzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A solution of(1aRS,7bSR)-5-(2-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid (Intermediate 67, 0.6 g) and (S)-1-azabicyclo[2.2.2]oct-3-ylamine(6.0 g) in DMSO (6 mL) was stirred and heated in a sealed vessel at 140°C. for 22 hours. After cooling, the mixture was diluted with methanoland concentrated under vacuum. The residue was purified by HPLC (C18) togive(1aRS,7bSR)-5-{2-[((S)-1-azabicyclo[2.2.2]oct-3-yl)amino]benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.107 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.58 (1H, ddd), 7.25 (1H, t), 6.94 (1H, dd), 6.76(2H, t), 6.62 (2H, m), 6.06 (1H, d), 4.14 (1H, t), 3.86 (1H, br s), 3.57(3H, m), 3.16-2.87 (4H, m), 2.12 (1H, m), 2.01 (1H, m), 1.82 (3H, m),1.65 (2H, m), 0.83 (1H, m), 0.67 (1H, m).

LCMS (Method C) r/t 3.16 (M+H) 470).

Example 74(1aRS,7bSR)-5-{2-[((R)-1-Azabicyclo[2.2.2]oct-3-yl)amino]benzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a similar manner to Example 73, starting from(1aRS,7bSR)-5-(2-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid (Intermediate 67) and (R)-1-azabicyclo[2.2.2]oct-3-ylamine.

¹H NMR (DMSO-d₆) δ: 7.58 (1H, ddd), 7.25 (1H, t), 6.94 (1H, dd), 6.76(2H, t), 6.62 (2H, m), 6.07 (1H, d), 4.13 (1H, t), 3.86 (1H, br s), 3.57(3H, m), 3.16-2.87 (4H, m), 2.12 (1H, m), 2.01 (1H, m), 1.83 (3H, m),1.64 (2H, m), 0.83 (1H, m), 0.67 (1H, m).

LCMS (Method C) r/t 3.15 (M+H) 470

Example 75(1aRS,7bSR)-5-(2-{[((S)-1-ethylpyrrolidine-3-carbonyl)amino]methyl}-4-fluoro-benzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Methyl(1aRS,7bSR)-5-(2-{[((S)-1-ethylpyrrolidine-3-carbonyl)amino]methyl}-4-fluoro-benzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 188, 0.190 g) and lithium hydroxide monohydrate (0.150 g)were suspended in dioxane (5 mL) and water (5 mL) and the mixture wasstirred and heated at 100° C. for 18.5 hours. After cooling, thevolatiles were removed in vacuo and the residue was acidified byaddition of aqueous citric acid solution (10%) and extracted with DCM.The organic layer was dried (Na₂SO₄) and filtered. The filtrate wasevaporated to dryness and the residue was purified by preparative HPLC(C18) eluting with a mixture of acetonitrile and water, containing 0.1%formic acid, with a gradient of 25-60% to give(1aRS,7bSR)-5-(2-{[((S)-1-ethylpyrrolidine-3-carbonyl)amino]methyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.092 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 8.78 (1H, q), 7.89-7.82 (1H, m), 7.19 (1H, td), 7.12(1H, dt), 7.02 (1H, dd), 6.75 (1H, dd), 4.74 (2H, d), 4.19 (1H, d), 3.62(1H, dt), 3.50-3.15 (5H, m), 3.10 (2H, q), 2.35-2.23 (1H, m), 2.10-1.99(1H, m), 1.86 (1H, dt), 1.75-1.67 (1H, m), 1.20 (3H, t), 0.90 (1H, dt),0.73 (1H, q)

LCMS (Method C) r/t 3.01 (M+H) 518

Example 76(1aRS,7bSR)-5-{2-[2-((R)-1-Ethylpyrrolidin-3-ylamino)ethyl]-4-fluoro-benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A solution of(1aRS,7bSR)-5-(4-fluoro-2-vinylbenzenesulfonylamino)-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylicacid (Intermediate 74, 0.150 g) and (R)-1-ethylpyrrolidin-3-ylamine(Intermediate 193, 0.25 g) in ethylene glycol (1 ml) was irradiated inthe microwave at 200° C. for 30 minutes. After cooling, the mixture wasdiluted with water and loaded onto a SCX-2 SPE cartridge then washedwith water, methanol and 2M ammonia in methanol. The basic fractionswere combined and evaporated to dryness. The residue was purified bypreparative HPLC (C18) eluting with a mixture of methanol and water,containing 0.1% ammonia, with a gradient of 10-98%. Then furtherpurified by preparative HPLC (C18) eluting with a mixture ofacetonitrile and water, containing 0.1% formic acid, with a gradient of10-60% to give(1aRS,7bSR)-5-{2-[2-((R)-1-ethylpyrrolidin-3-ylamino)ethyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylicacid (0.005 g) as a white solid.

¹H NMR (CDCl₃) δ: 7.86 (1H, dd), 7.43 (1H, dd), 7.31 (1H, dt), 7.27 (1H,d), 6.59 (1H, d), 4.31 (1H, d), 4.18-3.97 (1.5H, br), 3.82-3.64 (1.5H,br), 3.79 (1H, d), 3.33-3.20 (8H, br), 2.31 (1H, br s), 2.04 (1H, m),1.84 (1H, q), 1.26 (4H, t), 1.07 (1H, m), 0.86 (1H, q).

LCMS (Method C) r/t 2.60 (M+H) 503.9

Example 77(1aRS,7bSR)-5-{2-[((R)-1-Ethylpyrrolidin-3-yl)amino]benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A solution of(1aRS,7bSR)-5-(2-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid (Intermediate 67, 0.13 g) and (R)-1-ethylpyrrolidin-3-ylamine(Intermediate 193, 1.22 g) in DMSO (0.7 mL) was stirred and heated in asealed vessel at 120° C. for 22 hours. After cooling, the mixture wasdiluted with methanol and concentrated under vacuum. The residue waspurified by HPLC (C18) to give(1aRS,7bSR)-5-{2-[((S)-1-ethylpyrrolidin-3-yl)amino]benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.107 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.32 (2H, m), 7.04 (1H, d), 6.98 (1H, m), 6.72 (1H,d), 6.60 (1H, t), 5.55 (1H, br s), 4.18 (1H, br s), 4.11 (1H, t), 3.78(1H, br s), 3.66-3.48 (2H, m), 3.18-2.94 (4H, m), 2.54 (1H, m), 1.86(2H, m), 1.66 (1H, m), 1.22 (3H, t), 0.86 (1H, m), 0.68 (1H, m).

LCMS (Method C) r/t 3.40 (M+H) 458.

Example 78(1aRS,7bSR)-5-{2-[((S)-1-Ethylpyrrolidin-3-yl)amino]benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a similar manner to Example 77, starting from(1aRS,7bSR)-5-(2-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid (Intermediate 67) and (S)-1-ethylpyrrolidin-3-ylamine (Intermediate194).

¹H NMR (DMSO-d₆) δ: 7.32 (2H, m), 7.05 (1H, d), 6.98 (1H, m), 6.72 (1H,d), 6.60 (1H, t), 5.54 (1H, br s), 4.20 (1H, br s), 4.11 (1H, t), 3.80(1H, br s), 3.69-3.48 (2H, m), 3.19-2.96 (4H, m), 2.56 (1H, m), 1.86(2H, m), 1.66 (1H, m), 1.22 (3H, t), 0.87 (1H, m), 0.68 (1H, m).

LCMS (Method C) r/t 3.40 (M+H) 458.

Example 79(1aRS,7bSR)-5-(2-{[((R)-1-Ethylpyrrolidine-3-ylcarbonyl)amino]methyl}-4-fluoro-benzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of methyl(1aRS,7bSR)-5-(2-{[((R)-1-ethylpyrrolidine-3-ylcarbonyl)amino]methyl}-4-fluoro-benzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 195, 0.215 g) and lithium hydroxide monohydrate (0.170 g)was suspended in dioxane (5 mL) and water (5 mL) and the mixture wasstirred and heated at 80° C. for 21 hours. The temperature was raised to100° C. and the mixture was stirred and heated at that temperature for2.5 hours. Further lithium hydroxide monohydrate (0.05 g) was added andthe mixture was stirred and heated at 100° C. for 2 hours. Aftercooling, the volatiles were removed in vacuo and the residue wasacidified by addition of aqueous citric acid solution (10%) andextracted with DCM. The organic layer was dried (Na₂SO₄) and filtered.The filtrate was evaporated to dryness and the residue was purified bypreparative HPLC (C18) eluting with a mixture of acetonitrile and water,containing 0.1% formic acid, with a gradient of 25-60% to give(1aRS,7bSR)-5-(2-{[((R)-1-ethylpyrrolidine-3-ylcarbonyl)-amino]methyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.103 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 8.78 (1H, q), 7.89-7.83 (1H, m), 7.18 (1H, td), 7.11(1H, dt), 7.01 (1H, dd), 6.76 (1H, dd), 4.74 (2H, d), 4.19 (1H, d), 3.61(1H, dt), 3.46-3.12 (5H, m), 3.07 (2H, q), 2.34-2.22 (1H, m), 2.10-1.98(1H, m), 1.86 (1H, dt), 1.70 (1H, q), 1.19 (3H, t), 0.90 (1H, dt), 0.73(1H, q).

LCMS (Method C) r/t 3.04 (M+H) 518.

Example 80(1aRS,7bSR)5-[2-((Z)-3-Diethylamino-2-methylprop-1-enyl)-4-fluoro-benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of methyl(1aRS,7bSR)-5-{N-[2-((Z)-3-diethylamino-2-methylprop-1-enyl)-4-fluorobenzenesulfonyl]-N-methoxycarbonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(Intermediate 200, 0.264 g) and lithium hydroxide monohydrate (0.505 g)in dioxane (9 mL) and water (3 mL) was irradiated in the microwave at130° C. for 40 minutes. After cooling, the mixture was diluted withmethanol, acidified with formic acid and evaporated in vacuo thenazeotroped with a mixture of ethanol and toluene. The residue wastriturated with 15% methanol in DCM, filtered and the filtrate wasevaporated in vacuo. The residue was purified by chromatography onsilica, eluting with a mixture of methanol and DCM with a gradient of0-40%. The resultant solid was triturated with ether and filtered togive(1aRS,7bSR)-5-[2-((Z)-3-diethylamino-2-methylprop-1-enyl)-4-fluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.202 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.95 (1H, dd), 7.28 (1H, dt), 7.14 (1H, dd), 7.06(1H, d), 6.92 (1H, s), 6.64 (1H, d), 4.25 (1H, d), 3.64 (1H, d), 3.36(2H, br, s), 2.63 (4H, q), 1.96 (3H, s), 1.90 (1H, m), 1.74 (1H, m),0.93 (1H, m), 0.86 (6H, t), 0.75 (1H, m).

LCMS (Method C) r/t 3.27 (M+H) 489

Example 81(1aRS,7bSR)-5-{2-[2-((R)-1-Ethylpyrrolidin-3-yl)ethylamino]benzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of(1aRS,7bSR)-5-(2-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid (Intermediate 67, 0.2 g) and2-((R)-1-ethylpyrrolidin-3-yl)ethylamine (Intermediate 203, 2.0 g) inDMSO (2 mL) was divided between two sealed vials and each was stirredand heated at 130° C. for 24 hours. After cooling, the combined mixturewas diluted with methanol and then concentrated under vacuum. Theresidue was purified by HPLC (C18) to give(1aRS,7bSR)-5-{2-[2-((R)-1-ethylpyrrolidin-3-yl)ethylamino]-benzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.125 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.62 (1H, dt), 7.29 (1H, dt), 7.02 (2H, 2s), 6.70(1H, d), 6.58 (1H, t), 5.84 (1H, br m), 4.14 (1H, d), 3.54 (1H, d), 3.36(1H m), 3.18 (3H, m), 3.06 (4H, m), 2.59 (1H, m), 2.01 (1H, m), 1.83(1H, m), 1.80-1.49 (4H, m), 1.19 (3H, q), 0.85 (1H, m), 0.69 (1H, m).

LCMS (Method C) r/t 3.35 (M+H) 486.

Example 82(1aRS,7bSR)-5-{2-[2-((S)-1-Ethylpyrrolidin-3-yl)ethylamino]benzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a similar manner to Example 58, starting from(1aRS,7bSR)-5-(2-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid (Intermediate 67) and 2-((S)-1-ethylpyrrolidin-3-yl)ethylamine(Intermediate 208).

¹H NMR (DMSO-d₆) δ: 7.62 (1H, dt), 7.29 (1H, dt), 7.02 (2H, 2s), 6.70(1H, d), 6.57 (1H, t), 5.84 (1H, br m), 4.14 (1H, d), 3.54 (1H, d), 3.36(1H m), 3.17 (3H, m), 3.06 (4H, m), 2.57 (1H, m), 2.01 (1H, m), 1.83(1H, m), 1.80-1.49 (4H, m), 1.19 (3H, q), 0.85 (1H, m), 0.68 (1H, m).

LCMS (Method C) r/t 3.34 (M+H) 486.

Example 83(1aR,7bS)-5-[2-((S)-1-Ethylpyrrolidin-3-yloxymethyl)-4-fluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of methyl(1aR,7bS)-5-[2-((S)-1-ethylpyrrolidin-3-yloxymethyl)-4-fluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 213, 0.217 g) and lithium hydroxide monohydrate (0.168 g)in dioxane (3 mL) and water (1 mL) was irradiated in the microwave at130° C. for 40 minutes. After cooling, the mixture was diluted withmethanol, acidified with formic acid, evaporated in vacuo and azeotropedwith a mixture of toluene and ethanol. The residue was triturated with15% methanol in DCM, filtered and the filtrate was evaporated in vacuo.The residue was purified by chromatography on silica, eluting with amixture of methanol and DCM with a gradient of 0-20%. The resultant gumwas triturated with ether and ethyl acetate and filtered to give(1aR,7bS)-5-[2-((S)-1-ethylpyrrolidin-3-yloxymethyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.136 g) as a white solid.

¹H NMR (CDCl₃) δ: 7.35 (1H, dd), 7.23 (1H, d), 7.19 (1H, dd), 7.01 (1H,d), 6.83 (1H, dt), 4.87 (1H, br, d), 4.73 (1H, br, d), 4.36 (2H, br, m),4.19 (1H, d), 3.88 (1H, m), 3.84 (1H, d), 3.38 (1H, m), 2.94 (1H, m),2.86 (1H, m), 2.75 (1H, m), 2.26-2.45 (2H, m), 1.81 (1H, m), 1.60 (1H,m), 1.39 (3H, t), 0.90 (2H, m).

LCMS (Method C) r/t 3.25 (M+H) 491

Example 84(1aR,7bS)-5-[2-((R)-1-Ethylpyrrolidin-3-yloxymethyl)-4-fluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Prepared by proceeding in a similar manner to Example 83, starting frommethyl(1aR,7bS)-5-[2-((R)-1-ethylpyrrolidin-3-yloxymethyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate(Intermediate 217).

¹H NMR (DMSO-d₆) δ: 7.83 (1H, dd), 7.44 (1H, dd), 7.20 (1H, dt), 7.07(1H, d), 7.03 (1H, d), 4.99 (1H, d), 4.49 (2H, d), 4.19 (2H, d), 3.57(2H, d), 2.93-3.30 (4H, m), 2.34 (1H, m), 2.13 (1H, m), 1.88 (1H, m),1.72 (1H, m), 1.29 (3H, t), 0.92 (1H, m), 0.75 (1H, m).

LCMS (Method C) r/t 3.25 (M+H) 491.

Example 85 (1aR,7bS)-5-[2-(1-Ethylpiperidin-3-ylmethyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of methyl(1aR,7bS))-5-[2-(1-ethylpiperidin-3-ylmethyl)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 221, 0.071 g) and lithium hydroxide monohydrate (0.059 g)was suspended in dioxane (5 mL) and water (2 mL) and the mixture wasstirred and heated at 100° C. for 25 hours. Further lithium hydroxidemonohydrate (0.116 g) was added and the mixture was heated at 100° C.for a further 18 hours. After cooling, the volatiles were removed invacuo and the residue was acidified by addition of aqueous citric acidsolution (10%) and saturated with sodium chloride. The mixture wasextracted with DCM and the organic layer was dried (Na₂SO₄) andfiltered. The filtrate was evaporated to dryness and the residue waspurified by preparative HPLC (C18), eluting with a mixture ofacetonitrile and water, containing 0.1% formic acid, with a gradient of25-60% to give(1aR,7bS)-5-[2-(1-ethyl-piperidin-3-ylmethyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid (0.032 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 8.01-7.91 (1H, m), 7.26-7.18 (2H, m), 7.10-7.00 (2H,m), 4.22-4.17 (1H, m), 3.61 (1H, d), 3.45-2.92 (5H, m), 3.02-2.88 (4H,m), 1.94-1.85 (1H, m), 1.80-1.65 (3H, m), 1.65-1.50 (1H, m), 1.30-1.14(4H, m), 0.97-0.87 (1H, m), 0.77-0.68 (1H, m).

LCMS (Method C) r/t 3.21 (M+H) 489.

Example 86(1aR,7bS)-5-{2-[2-((R)-1-Ethylpyrrolidin-2-yl)ethyl]-4-fluorobenzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Lithium hydroxide (0.22 g) was added to a solution of methyl(1aR,7bS)-5-{2-[2-((R)-1-ethyl-pyrrolidin-2-yl)ethyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(Intermediate 229, 0.26 g) in a mixture of dioxane (12 mL) and water (4mL) and the mixture was irradiated in a microwave at 150° C. for 20minutes. After cooling, the mixture was evaporated to dryness and theresidue was acidified by addition of 10% aqueous citric acid (3 mL) andthen extracted with DCM. The organic layer was dried (MgSO₄) andfiltered and the filtrate was evaporated to dryness. The residue waspurified by preparative HPLC (C18) eluting with a mixture ofacetonitrile and water, containing 0.1% formic acid, with a gradient of25-35% to give(1aR,7bS)-5-{2-[2-((R)-1-ethylpyrrolidin-2-yl)ethyl]-4-fluoro-benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.11 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.88 (1H, dd), 7.33 (1H, dd), 7.15 (1H, dt), 7.08(1H, d), 6.98 (1H, d), 4.18 (1H, d), 3.68 (1H, br m), 3.58 (1H, d), 3.56(1H, m), 3.22-2.96 (5H, m), 2.23 (1H, m), 2.03 (4H, m), 1.87 (2H, m),1.72 (1H, q), 1.31 (3H, t), 0.91 (1H, m), 0.72 (1H, q).

LCMS (Method C) r/t 3.24 (M+H) 489.

Intermediate 1: Methylcis-(3aRS,9bRS)-7-(benzenesulfonylamino)-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate

Formic acid (5 mL) was added to methylcis-(3aRS,9bRS)-7-[bis-(tert-butoxycarbonyl)amino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate(Intermediate 2, 0.15 g) and the mixture was stirred at room temperaturefor 1 hour. The resultant mixture was evaporated to dryness and theresidue was redissolved in toluene and evaporated to dryness threetimes. The residue was dissolved in DCM (2 mL) and pyridine (1 mL) wasadded followed by benzenesulfonyl chloride (0.07 g). The resultantmixture was stirred at room temperature for 90 minutes then diluted withDCM and washed with sodium hydroxide (1M) and brine. The sodiumhydroxide washing was saturated with salt and then extracted with ethylacetate, dried (MgSO₄) and filtered. The filtrate was evaporated todryness to give methylcis-(3aRS,9bRS)-7-(benzenesulfonylamino)-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate(0.082 g) as a gum.

¹H NMR (CDCl₃) δ: 7.73 (2H, dd), 7.53 (1H, t), 7.42 (2H, t), 7.25 (1H,d), 7.21 (1H, d), 4.29 (1H, m), 4.03 (1H, dd), 3.93 (1H, dd), 3.82 (2H,t), 3.70 (3H, s), 3.45 (1H, m), 2.48 (1H, m), 1.87 (1H, m).

Intermediate 2: Methylcis-(3aRS,9bRS)-7-[bis-(tert-butoxycarbonyl)amino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate

A solution of methyl7-[bis-(tert-butoxycarbonyl)amino]-4H-furo[2,3-c]-chromene-6-carboxylate(Intermediate 3, 0.15 g) in a mixture of dioxane (15 mL) and acetic acid(1.5 mL) was treated under an atmosphere of nitrogen with palladium oncarbon (10%, 0.02 g). The mixture was stirred and the nitrogen wasreplaced by hydrogen then the mixture was stirred under an atmosphere ofhydrogen for 3 hours. The mixture was filtered through Celite, the padwas washed thoroughly with dioxane and the filtrate was evaporated todryness to give methylcis-(3aRS,9bRS)-7-[bis-(tert-butoxycarbonyl)amino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate(0.15 g) as a gum.

¹H NMR (CDCl₃) δ: 7.22 (1H, dd), 6.80 (1H, d), 4.36 (1H, m), 4.07 (2H,d), 3.86 (2H, t), 3.84 (3H, s), 3.53 (1H, m), 2.50 (1H, m), 1.94 (1H,m), 1.40 (18H, s).

Intermediate 3: Methyl7-[bis-(tert-butoxycarbonyl)amino]-4H-furo[2,3-c]-chromene-6-carboxylate

Carbon tetrabromide (2.66 g) was added to a solution of methyl6-[bis-(tert-butoxycarbonyl)amino]-2-hydroxy-3-(2-hydroxymethylfuran-3-yl)-benzoate(Intermediate 4, 2.65 g) and triphenyl phosphine (2.1 g) in DCM (40 mL)and the resultant solution was stirred at room temperature for 1 hour.The mixture was evaporated to dryness and DMF (60 mL) and cesiumcarbonate (5.59 g) were added to the residue. The resultant mixture wasstirred for 1 hour, then partitioned between ethyl acetate and water.The organic layer was separated, dried (Na₂SO₄) and filtered. Thefiltrate was evaporated to dryness and the residue was purified bychromatography on silica, eluting with a mixture of ethyl acetate andcyclohexane with a gradient of 5-25% to give methyl7-[bis-(tert-butoxycarbonyl)amino]-4H-furo[2,3-c]-chromene-6-carboxylate(0.735 g) as a gum which crystallised on standing.

¹H NMR (CDCl₃) □δ: 7.45 (1H, m), 7.26 (1H, s), 6.79 (1H, d), 6.65 (1H,d), 5.44 (2H, s), 3.87 (3H, s), 1.42 (18H, s).

Intermediate 4: Methyl6-[bis-(tert-butoxycarbonyl)amino]-2-hydroxy-3-(2-hydroxymethylfuran-3-yl)benzoate

1M aqueous sodium hydroxide (50 mL) was added to a solution of methyl6-[bis-(tert-butoxycarbonyl)amino]-3-(2-hydroxymethylfuran-3-yl)-2-(4-methylbenzene-sulfonyloxy)benzoate(Intermediate 5, 3.82 g) in methanol (100 mL) and the mixture wasstirred and heated at 45° C. for 1.5 hours. The mixture was evaporatedto dryness and the residue was dissolved in ethyl acetate and acidifiedwith acetic acid. The organic layer was separated, dried (Na₂SO₄) andfiltered. The filtrate was evaporated to dryness and the residue waspurified by chromatography on silica, eluting with a mixture of ethylacetate and cyclohexane with a gradient of 10-50% to give methyl6-[bis-(tert-butoxycarbonyl)amino]-2-hydroxy-3-(2-hydroxymethylfuran-3-yl)benzoate(2.65 g) as a white foam.

¹H NMR (CDCl₃) δ: 11.91 (1H, s), 7.50 (2H, m), 6.80 (1H, d), 6.57 (1H,d), 4.58 (2H, s), 3.97 (3H, s), 1.43 (18H, s).

Intermediate 5: Methyl6-[bis-(tert-butoxycarbonyl)amino]-3-(2-hydroxymethyl-furan-3-yl)-2-(4-methylbenzenesulfonyloxy)benzoate

Sodium borohydride (0.304 g) was added to a solution of methyl6-[bis-(tert-butoxycarbonyl)amino]-3-(2-formylfuran-3-yl)-2-(4-methylbenzenesulfonyloxy)-benzoate(Intermediate 6, 3.9 g) in ethanol (50 mL) and the mixture was stirredfor 15 minutes. The mixture was evaporated to dryness and the residuewas partitioned between ethyl acetate and water. The organic layer wasseparated, dried (Na₂SO₄) and filtered. The filtrate was evaporated todryness to give methyl6-[bis-(tert-butoxycarbonyl)amino]-3-(2-hydroxymethylfuran-3-yl)-2-(4-methylbenzene-sulfonyloxy)benzoate(3.82 g) as a white solid.

¹H NMR (CDCl₃) δ: 7.40 (1H, d), 7.38 (2H, d), 7.30 (1H, d), 7.18 (1H,d), 7.11 (2H, d), 6.28 (1H, d), 4.33 (2H, s), 3.82 (3H, s), 2.40 (3H,s), 1.42 (18H, s).

Intermediate 6: Methyl6-[bis-(tert-butoxycarbonyl)amino]-3-(2-formylfuran-3-yl)-2-(4-methylbenzenesulfonyloxy)benzoate

Triethylamine (0.848 g) was added to a stirred solution of methyl6-amino-3-(2-formylfuran-3-yl)-2-hydroxybenzoate (Intermediate 7, 1.72g), 4-methylbenzenesulfonyl chloride (1.25 g) and DMAP (0.804 g) in DCM(30 mL) and the resultant mixture was stirred for 1 hour. The mixturewas diluted with water and the organic layer was separated, dried(Na₂SO₄) and filtered. The filtrate was evaporated to dryness and theresidue was dissolved in acetonitrile (30 mL) and DMAP (0.804 g) anddi-tert-butyl dicarbonate (3.16 g) were added. The mixture was stirredfor 2 hours then diluted with ethyl acetate and water. The organic layerwas separated, dried (Na₂SO₄) and filtered. The filtrate was evaporatedto dryness and the residue was purified by chromatography on silica,eluting with a mixture of ethyl acetate and cyclohexane with a gradientof 10-50% to give methyl6-[bis-(tert-butoxycarbonyl)amino]-3-(2-formylfuran-3-yl)-2-(4-methylbenzenesulfonyloxy)-benzoate(3.91 g) as a white foam.

¹H NMR (CDCl₃) δ: 9.13 (1H, d), 7.54 (1H, dd), 7.38 (1H, d), 7.31 (2H,d), 7.23 (1H, d), 7.05 (2H, d), 6.75 (1H, d), 3.94 (3H, s), 2.37 (3H,s), 1.45 (18H, s).

Intermediate 7: Methyl 6-amino-3-(2-formylfuran-3-yl)-2-hydroxybenzoate

A mixture of methyl 6-amino-3-bromo-2-hydroxybenzoate (preparedaccording to Wang et al, Bioorg Med Chem Let, t 2007, 17, 2817; 1.84 g),2-formylfuran-3-boronic acid pinacol ester (1.99 g),tri-tert-butylphosphonium tetrafluoroborate (0.218 g), cesium carbonate(7.33 g) and tris-(dibenzylideneacetone)dipalladium (0.343 g) in dioxane(75 mL) and water (9.4 mL) was heated at 65° C., under nitrogen, for 1hour. After cooling, the mixture was diluted with ethyl acetate andwater and the organic layer was separated, dried (Na₂SO₄) and filtered.The filtrate was evaporated to dryness and the residue was purified bychromatography on silica, eluting with a mixture of ethyl acetate andcyclohexane with a gradient of 10-50% to give methyl6-amino-3-(2-formylfuran-3-yl)-2-hydroxybenzoate (1.72 g) as a yellowsolid. The material was used without further characterisation.

Intermediate 8:7-[2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzene-sulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylicacid

Methyl7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylate(Intermediate 9, 0.129 g) was added to a solution of lithium hydroxidemonohydrate (0.42 g) in water (2 mL) and dioxane (8 mL), and the mixturewas irradiated in the microwave at 130° C. for 1 hour. After cooling,the mixture was acidified with formic acid, and evaporated to dryness.The residue was triturated with 10% methanol in DCM, filtered and thefiltrate was evaporated to dryness. The residue was purified bychromatography on silica, eluting with a mixture of methanol and DCMwith a gradient of 0-10%. The isolated product was triturated with ethylacetate and the solid was collected by filtration and dried in vacuo togive7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylicacid (0.056 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.71 (1H, d), 7.68 (1H, d), 7.38 (1H, d), 7.28 (1H,dd), 7.26-7.19 (2H, m), 7.02 (1H, d), 6.86 (1H, d), 6.20-6.11 (1H, m),5.28 (2H, s), 3.79 (2H, d), 3.12 (4H, q), 1.14 (6H, t).

LCMS (Method C) r/t 3.48 (M+H) 501.

Intermediate 9: Methyl7-[2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzene-sulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylate

A mixture of methyl7-(2-bromo-4-fluorobenzenesulfonylamino)-4H-furo[2,3-c]chromene-6-carboxylate(Intermediate 10, 2.04 g),N,N-diethyl-N—((Z)-1-tributylstannanylprop-1-en-3-yl)amine (Intermediate11, 3.4 g), tri-tert-butylphosphonium tetrafluoroborate (0.246 g),tris-(dibenzylideneacetone)dipalladium (0.0.388 g) in dioxane (35 mL)was degassed and purged with argon then heated at 100° C. for 3.5 hours.After cooling, the mixture was diluted with ethyl acetate and filtered.The filtrate was washed with water, dried (Na₂SO₄) and filtered. Thefiltrate was evaporated to dryness and the residue was purified bychromatography on silica, eluting with a mixture of ammonia in methanol(2M) and DCM with a gradient of 0-10%. The product was triturated withether and the solid was collected by filtration to give methyl7-[2-((Z)-3-diethylaminoprop-1-en-1-yl)-4-fluorobenezenesulfonyl-amino]-4H-furo[2,3-c]chromene-6-carboxylate(1.47 g) as a pale orange solid.

¹H NMR (CDCl₃) δ: 8.06 (1H, dd), 7.40 (1H, m), 7.17 (1H, d), 7.14-6.98(2H, m), 7.0-6.9 (2H, m), 6.56 (1H, d), 6.06 (1H, m), 5.37 (2H, s), 3.87(3H, s), 3.17 (2H, m), 2.55 (4H, m), 0.97 (6H, t).

Intermediate 10: Methyl7-(2-bromo-4-fluorobenzenesulfonylamino)-4H-furo[2,3-c]chromene-6-carboxylate

Methyl7-[bis-(tert-butoxycarbonyl)amino]-4H-furo[2,3-c]-chromene-6-carboxylate(Intermediate 3, 2.66 g) was dissolved in formic acid (50 mL) and themixture was stirred at room temperature for 90 minutes. The mixture wasevaporated to dryness and the crude residue was partitioned betweenethyl acetate and aqueous potassium carbonate solution (10%). Theorganic layer was separated, dried (MgSO₄) and filtered. The filtratewas evaporated to dryness and the residue was dissolved in DCM (20 mL)and pyridine (10 mL) and 2-bromo-4-fluorobenzenesulfonyl chloride (1.95g) was added. The resultant mixture was stirred for 3.5 hours thenevaporated to dryness. The residue was dissolved in DCM washed withwater and filtered through a phase separator. The filtrate wasevaporated to dryness and the residue was purified by chromatography onsilica, eluting with a mixture of ethyl acetate and cyclohexane with agradient of 0-60% to give methyl7-(2-bromo-4-fluorobenzenesulfonyl-amino)-4H-furo[2,3-c]chromene-6-carboxylate(0.47 g) as a pale yellow solid.

¹H NMR (CDCl₃) δ: 9.25 (1H, br s), 8.14 (1H, dd), 7.40 (2H, m), 7.16(2H, m), 7.12 (1H, m), 6.55 (1H, d), 5.36 (2H, s), 3.92 (3H, s).

Intermediate 11:N,N-Diethyl-N—((Z)-1-tributylstannanylprop-1-en-3-yl)-amine

Diethylamine (19 mL) was added to a solution of((Z)-3-bromoprop-1-enyl)-tributylstannane (Intermediate 12, 7.52 g) inTHF (60 mL) and the mixture was stirred for 3 hours. The reactionmixture was evaporated to dryness and the residue was purified bychromatography on a silica column which had been pre-washed with 20%triethylamine in acetonitrile. The column was eluted with a mixture ofethyl acetate and pentane with a gradient of 0-10% to giveN,N-diethyl-N—((Z)-1-tributylstannanylprop-1-en-3-yl)amine (4.75 g) asan orange oil.

¹H NMR (CDCl₃) δ: 6.59 (1H, dt), 5.97 (1H, dt), 3.08 (2H, dd), 2.53 (4H,q), 1.49 (6H, m), 1.37-1.24 (6H, m), 1.04 (6H, t), 0.92-0.89 (15H, m).

Intermediate 12: ((Z)-3-Bromoprop-1-enyl)-tributylstannane

A solution of triphenylphosphine (5.32 g) in DCM (60 mL) was added to asolution of (Z)-3-tributylstannanylprop-2-en-1-ol (Intermediate 13, 6.4g) and carbon tetrabromide (9.18 g) in DCM (60 mL) and the mixture wasstirred for 2.5 hours. The mixture was evaporated to low volume andpentane was added. The solids were removed by filtration and thefiltrate was evaporated to dryness. Pentane was added and the solidswere again removed by filtration and the filtrate was evaporated todryness to give ((Z)-3-bromoprop-1-enyl)-tributylstannane (12.14 g) asan oil.

¹H NMR (CDCl₃) δ: 6.71 (1H, dt), 6.11 (1H, d), 3.88 (2H, d), 1.52-1.50(6H, m), 1.37-1.27 (6H, m), 0.99-0.97 (6H, m), 0.90 (9H, t).

Intermediate 13: (Z)-3-Tributylstannanylprop-2-en-1-ol

Propargyl alcohol (5 mL) was added to a solution of lithium aluminiumhydride (1M in THF, 43 mL) in THF (70 mL) at −78° C. The resultantmixture was warmed to room temperature and stirred for 18 hours. It wasre-cooled to −78° C. and a solution of tri-n-butyl tin chloride (8.32mL) in diethyl ether (50 mL) was added and the mixture was stirred for 3hours whilst gradually warming to room temperature. The reaction mixturewas cooled to −5° C. and quenched by addition of water and 15% aqueoussodium hydroxide solution then warmed to room temperature. Ethyl acetatewas added and the mixture was stirred for 1 hour. The mixture wasfiltered through Celite and the filtrate was evaporated to dryness. Theresidue was purified by chromatography on a silica column which had beenpre-washed with 20% triethylamine in acetonitrile. The column was elutedwith a mixture of ethyl acetate and pentane with a gradient of 0-10% togive (Z)-3-tributylstannanyl-prop-2-en-1-ol (5.06 g) as a clear oil.

¹H NMR (CDCl₃) δ: 6.70 (1H, dt), 6.08 (1H, dt), 4.12 (2H, dd), 1.49 (6H,m), 1.31 (6H, m), 0.98-0.84 (15H, m).

Intermediate 14: Methylcis-(3aRS,9bRS)-7-[2-(3-{pyrrolidin-1-yl}propyl)-4-fluorobenzenesulfonylamino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate

A solution of methyl7-[2-((Z)-3-{pyrrolidin-1-yl}prop-1-enyl)-4-fluorobenzene-sulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylate(Intermediate 15, 0.06 g) in IMS (4 mL) and formic acid (2 drops) wastreated under an atmosphere of nitrogen with palladium hydroxide oncarbon (10%, 0.02 g). The nitrogen was replaced by hydrogen and themixture was stirred under an atmosphere of hydrogen for 1 hour. Themixture was filtered through Celite and the filtrate was evaporated todryness to give methylcis-(3aRS,9bRS)-7-[2-(3-{pyrrolidin-1-yl}propyl)-4-fluorobenzene-sulfonylamino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate(0.06 g) which was used without further characterisation.

Intermediate 15: Methyl7-[2-((Z)-3-{pyrrolidin-1-yl)}prop-1-enyl)-4-fluorobenzene-sulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylate

Prepared by proceeding in a similar manner to Intermediate 9, startingfrom methyl7-(2-bromo-4-fluorobenzenesulfonylamino)-4H-furo[2,3-c]chromene-6-carboxylate(Intermediate 10) and 1-((Z)-3-tributylstannanylallyl)pyrrolidine(Intermediate 16).

¹H NMR (CD₃OD) δ: 8.02 (1H, dd), 7.51 (1H, m), 7.16 (2H, d), 7.11-7.01(2H, m), 6.76 (1H, d), 6.69 (1H, d), 5.93-5.83 (1H, m), 5.31 (2H, s),3.80 (3H, s), 3.37-3.33 (2H, m), 2.69 (4H, m), 1.78 (4H, m).

Intermediate 16: 1-((Z)-3-tributylstannanylallyl)pyrrolidine

Prepared by proceeding in a similar manner to Intermediate 11 startingfrom ((Z)-3-bromoprop-1-enyl)tributylstannane (Intermediate 12) andpyrrolidine.

¹H NMR (CDCl₃) δ: 6.64 (1H, dt), 5.96 (1H, dt), 3.10 (2H, dd), 2.51 (4H,m), 1.79-1.78 (4H, m), 1.54-1.45 (6H, m), 1.36-1.26 (6H, m), 0.91-0.88(15H, t).

Intermediate 17: Methylcis-(3aRS,9bRS)-7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate

Prepared by proceeding in a similar manner to Intermediate 9, startingfrom methylcis-(3aRS,9bRS)-7-(2-bromo-4-fluorobenzenesulfonylamino)-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate(Intermediate 18) andN,N-diethyl-N—((Z)-1-tributylstannanylprop-1-en-3-yl)-amine(Intermediate 11) and heating at 80° C. for 2 hours.

LCMS (Method A) r/t 2.25 (M+H) 519.

Intermediate 18: Methylcis-(3aRS,9bRS)-7-(2-bromo-4-fluorobenzenesulfonyl-amino)-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate

2-Bromo-4-fluorobenzenesulfonyl chloride (0.335 g) was added to asolution of methyl cis-(3aRS,9bRS)-7-amino-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate(Intermediate 19, 0.255 g) in DCM (4 mL) and pyridine (2 mL) and theresultant mixture was stirred at room temperature overnight. The mixturewas evaporated to dryness and the residue was purified by chromatographyon silica eluting with a mixture of ethyl acetate and cyclohexane with agradient of 0-100% to give methylcis-(3aRS,9bRS)-7-(2-bromo-4-fluorobenzenesulfonylamino)-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate(0.486 g) as a yellow gum.

¹H NMR (CDCl₃) δ: 9.47 (1H, s), 8.17 (1H, m), 7.42 (1H, dd), 7.12 (1H,dt), 7.11 (2H, s), 4.28 (1H, m), 4.06 (1H, dd), 3.96 (1H, dd), 3.91 (3H,s), 3.82 (2H, m), 3.41 (1H, m), 2.45 (1H, m), 1.84 (1H, m).

Intermediate 19: Methylcis-(3aRS,9bRS)-7-amino-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate

Trifluoroacetic acid (7 mL) was added to a solution of methylcis-(3aRS,9bRS)-7-[bis-(tert-butoxycarbonyl)amino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate(Intermediate 2, 0.66 g) in DCM (15 mL) and the mixture was stirred atroom temperature for 1 hour. The mixture was evaporated to dryness andthe residue was treated with aqueous sodium bicarbonate and extractedwith DCM, dried (MgSO₄) and filtered. The filtrate was evaporated todryness to give methylcis-(3aRS,9bRS)-7-amino-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate(0.255 g) as a gum.

¹H NMR (CDCl₃) δ: 7.0 (1H, dd), 6.31 (1H, d), 4.32 (1H, m), 4.01 (2H,m), 3.88 (3H, s), 3.84 (2H, m), 3.39 (1H, m), 2.41 (1H, m), 1.86 (1H,m).

Intermediate 20: Methyl7-[N-{2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluoro-benzenesulfonyl}-N-(methoxycarbonyl)amino]-1,2-dihydrofuro[2,3-c]quinoline-6-carboxylate

Prepared by proceeding in a similar manner to Intermediate 9, startingfrom methyl7-[N-(2-bromo-4-fluorobenzenesulfonyl)-N-(methoxycarbonyl)amino]-1,2-dihydro-furo[2,3-c]quinoline-6-carboxylate(Intermediate 21) andN,N-diethyl-N—((Z)-1-tributylstannanylprop-1-en-3-yl)amine (Intermediate11) and heating at 60° C. for 1 hour.

¹H NMR (CDCl₃) δ: 8.72 (1H, s), 8.32 (1H, dd), 7.76 (1H, d), 7.62 (1H,d), 7.22-7.08 (3H, m), 6.03 (1H, m), 4.87 (2H, t), 3.93 (3H, s), 3.62(3H, s), 3.56 (2H, t), 3.20 (2H, m), 2.52 (4H, m), 0.97 (6H, t).

Intermediate 21: Methyl7-[N-(2-bromo-4-fluorobenzenesulfonyl)-N-(methoxy-carbonyl)amino]-1,2-dihydrofuro[2,3-c]quinoline-6-carboxylate

A solution of methyl7-(2-bromo-4-fluorobenzenesulfonylamino)-1,2-dihydro-furo[2,3-c]quinoline-6-carboxylate(Intermediate 22, 0.29 g) in THF (5 mL) was added slowly to a suspensionof sodium hydride (40% oil dispersion, 0.048 g) in THF (15 mL). Once theevolution of hydrogen had ceased, methyl chloroformate (0.147 g) wasadded and the mixture was stirred at room temperature for 1 hour. Themixture was diluted with ethyl acetate, washed with saturated sodiumbicarbonate solution, dried (MgSO₄) and filtered. The filtrate wasevaporated to dryness and the residue was triturated with a mixture ofether and cyclohexane (1:1) and the solid was collected by filtration togive methyl7-[N-(2-bromo-4-fluorobenzenesulfonyl)-N-(methoxy-carbonyl)amino]-1,2-dihydrofuro[2,3-c]quinoline-6-carboxylate(0.3 g) as a pale orange solid.

¹H NMR (CDCl₃) δ: 8.73 (1H, s), 8.48 (1H, dd), 7.76 (2H, s), 7.51 (1H,dd), 7.25 (1H, m), 4.86 (2H, t), 4.01 (3H, s), 3.66 (3H, s), 3.56 (2H,t).

Intermediate 22: Methyl7-(2-bromo-4-fluorobenzenesulfonylamino)-1,2-dihydro-furo[2,3-c]quinoline-6-carboxylate

Prepared by proceeding in a similar manner to Intermediate 18, startingfrom methyl 7-amino-1,2-dihydrofuro[2,3-c]quinoline-6-carboxylate(Intermediate 23) and 2-bromo-4-fluorobenzenesulfonyl chloride andstirring at room temperature for 3 days.

¹H NMR (CDCl₃) δ: 8.60 (1H, s), 8.07 (1H, dd), 7.84 (1H, d), 7.62 (1H,d), 7.43 (1H, dd), 7.06 (1H, m), 4.79 (2H, t), 4.02 (3H, s), 3.48 (2H,t).

Intermediate 23: Methyl7-amino-1,2-dihydrofuro[2,3-c]quinoline-6-carboxylate

A solution of methyl 7-aminofuro[2,3-c]quinoline-6-carboxylate(Intermediate 24, 1.13 g) in a mixture of dioxane (5 mL) and acetic acid(5 mL) was treated under an atmosphere of nitrogen with palladiumhydroxide on carbon (10%, 0.1 g). The nitrogen was replaced by hydrogenand the mixture was stirred under an atmosphere of hydrogen for 24hours. The mixture was diluted with ethyl acetate and filtered throughCelite and the filtrate was washed with 1M aqueous sodium hydroxidesolution, dried (MgSO₄) and filtered. The filtrate was evaporated todryness and the residue was purified by chromatography on silica elutingwith a mixture of methanol and ethyl acetate with a gradient of 0-10%.The isolated product was triturated with a mixture of ether andcyclohexane and the solid was collected by filtration to give methyl7-amino-1,2-dihydrofuro[2,3-c]quinoline-6-carboxylate (0.666 g) as ayellow solid.

¹H NMR (CDCl₃) δ: 8.56 (1H, s), 7.51 (1H, d), 6.95 (1H, d), 5.16 (2H, brs), 4.74 (2H, t), 4.05 (3H, s), 3.46 (2H, t).

Intermediate 24: Methyl 7-aminofuro[2.3-c]quinoline-6-carboxylate

A mixture of methyl 3-bromo-2,6-diaminobenzoate (Intermediate 25, 1.34g), 2-formylfuran-3-boronic acid pinacol ester (1.46 g),tri-tert-butylphosphonium tetrafluoroborate (0.305 g), cesium carbonate(5.15 g) and tris-(dibenzylideneacetone)dipalladium (0.49 g) in amixture of dioxane (80 mL) and water (30 mL) was degassed and purgedwith argon then heated at 60° C. for 1 hour. After cooling, the mixturewas filtered through Celite and the pad was washed thoroughly with ethylacetate. The filtrate was washed with water, dried (MgSO₄) and filtered.The filtrate was evaporated to dryness and the residue was purified bychromatography on silica eluting with a mixture of ethyl acetate andcyclohexane with a gradient of 0-100% to give methyl7-aminofuro[2,3-c]quinoline-6-carboxylate (1.13 g) as a brown gum.

¹H NMR (CDCl₃) δ: 9.11 (1H, s), 7.95 (1H, d), 7.82 (1H, d), 7.14 (1H,dd), 7.05 (1H, d), 5.05 (2H, br s), 4.08 (3H, s).

Intermediate 25: Methyl 3-bromo-2,6-diaminobenzoate

Iron powder (4.07 g) was added slowly with stirring and cooling to asolution of methyl 6-amino-3-bromo-2-nitrobenzoate (prepared accordingto Brock et al, Tetrahedron, 1963, 19, 1911; 2.0 g) in a mixture ofabsolute ethanol (49 mL), acetic acid (5 mL), formic acid (0.7 mL) andwater (15 mL). On completion of the addition, the mixture was stirred atroom temperature for 2 hours. The mixture was diluted with DCM and water(1:1) then filtered through Celite. The layers were separated and theaqueous layer was extracted with DCM. The combined organic layers werewashed with 1M aqueous sodium hydroxide solution, dried (MgSO₄) andfiltered. The filtrate was evaporated to dryness and the residue wastriturated with ether and cyclohexane (1:1) and the solid was collectedby filtration to give methyl 3-bromo-2,6-diaminobenzoate (1.34 g) as apale yellow solid.

¹H NMR (CDCl₃) δ: 7.21 (1H, d), 6.11 (2H, br s), 5.88 (1H, d), 5.46 (2H,br s), 3.93 (3H, s).

Intermediate 26: Methyl7-(benzenesulfonylamino)-1,2-dihydro[furo[2,3-c]quinoline-6-carboxylate

Prepared by proceeding in a similar manner to Intermediate 18, startingfrom methyl 7-amino-1,2-dihydrofuro[2,3-c]quinoline-6-carboxylate(Intermediate 23) and benzenesulfonyl chloride and stirring at roomtemperature overnight.

¹H NMR (CDCl₃) δ: 8.59 (1H, s), 7.94 (1H, d), 7.70 (1H, d), 7.50 (1H,m), 7.40 (2H, t), 7.21 (2H, m), 4.81 (2H, t), 3.75 (3H, s), 3.51 (2H,t).

Intermediate 27: Methylcis-(3aRS,9bRS)-5-acetyl-7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,2,3a,4,5,9b-hexahydrofuro[2,3-c]quinoline-6-carboxylate

Prepared by proceeding in a similar manner to Intermediate 9, startingfrom methylcis-(3aRS,9bRS)-5-acetyl-7-(2-bromo-4-fluorobenzenesulfonylamino)-1,2,3a,4,5,9b-hexahydrofuro[2,3-c]quinoline-6-carboxylate(Intermediate 28) and heating at 80° C. for 2 hours.

LCMS (Method B) r/t 2.29 (M+H) 560.

Intermediate 28: Methylcis-(3aRS,9bRS)-5-acetyl-7-(2-bromo-4-fluorobenzene-sulfonylamino)-1,2,3a,4,5,9b-hexahydrofuro[2,3-c]quinoline-6-carboxylate

Prepared by proceeding in a similar manner to Intermediate 18, startingfrom methylcis-(3aRS,9bRS)-5-acetyl-7-amino-1,2,3a,4,5,9b-hexahydrofuro[2,3-c]quinoline-6-carboxylate(Intermediate 29) and 2-bromo-4-fluorobenzenesulfonyl chloride.

¹H NMR (CDCl₃) δ: 9.51 (1H, br s), 8.16 (1H, m), 7.42 (1H, dd), 7.34(1H, d), 7.18 (1H, d), 7.12 (1H, dt), 4.46 (1H, d), 3.84 (2H, m), 3.81(3H, s), 3.67 (1H, m), 3.49 (1H, m), 3.38-3.19 (1H, m), 2.41-2.30 (1H,m), 2.25 (3H, s), 1.57 (1H, m).

Intermediate 29: Methylcis-(3aRS,9bRS)-5-acetyl-7-amino-1,2,3a,4,5,9b-hexahydrofuro[2,3-c]quinoline-6-carboxylate

Concentrated sulfuric acid (5 drops) was added to a solution of methylcis-(3aRS,9bRS)-5-acetyl-7-(2,2-dimethylpropionylamino)-1,2,3a,4,5,9b-hexahydro-furo[2,3-c]quinoline-6-carboxylate(Intermediate 30, 0.15 g) in methanol (5 mL) and the solution wasstirred and heated at reflux for 48 hours. After cooling, the mixturewas evaporated to low volume and the residue was dissolved in ethylacetate and carefully washed with saturated aqueous sodium bicarbonatesolution. The organic layer was filtered through a phase separator andthe filtrate was evaporated to dryness to give methylcis-(3aRS,9bRS)-5-acetyl-7-amino-1,2,3a,4,5,9b-hexahydrofuro[2,3-c]quinoline-6-carboxylate(0.09 g) as a brown gum.

¹H NMR (CDCl₃) δ: 7.04 (1H, d), 6.53 (1H, d), 4.97 (2H, br s), 4.47 (1H,m), 3.90 (2H, m), 3.79 (3H, s), 3.67 (1H, m), 3.45 (1H, m), 3.30 (1H,m), 2.4-2.32 (1H, m), 2.27 (3H, s), 1.68-1.54 (1H, m).

Intermediate 30: Methylcis-(3aRS,9bRS)-5-acetyl-7-(2,2-dimethylpropionylamino)-1,2,3a,4,5,9b-hexahydrofuro[2,3-c]quinoline-6-carboxylate

Sodium hydride (60% oil dispersion, 0.02 g) was added to a solution ofmethyl2-acetylamino-6-(2,2-dimethylpropionylamino)-3-[cis-(2RS,3RS)-2-(methanesulfonyl-oxymethyl)tetrahydrofuran-3-yl]benzoate(Intermediate 31, 0.166 g) in THF (3 mL) and the mixture was stirred atroom temperature for 20 minutes. A saturated aqueous solution ofammonium chloride was added and the mixture was extracted with DCM,dried (MgSO₄) and filtered. The filtrate was evaporated to dryness togive methylcis-(3aRS,9bRS)-5-acetyl-7-(2,2-dimethylpropionylamino)-1,2,3a,4,5,9b-hexahydrofuro[2,3-c]quinoline-6-carboxylate(0.15 g) as a tan coloured solid.

¹H NMR (CDCl₃) δ: 9.92 (1H, s), 8.29 (1H, d), 7.30 (1H, d), 4.51 (1H,d), 3.82 (3H, s), 3.75 (2H, m), 3.69 (1H, m), 3.56 (1H, m), 3.37-3.27(1H, br m), 2.44-2.34 (1H, br m), 2.29 (3H, s), 1.68-1.58 (1H, br m),1.29 (9H, s).

Intermediate 31: Methyl2-acetylamino-6-(2,2-dimethylpropionylamino)-3-[cis-(2RS,3RS)-2-(methanesulfonyloxymethyl)tetrahydrofuran-3-yl]benzoate

Methanesulfonyl chloride (0.042 mL) was added to a mixture of methyl2-acetylamino-6-(2,2-dimethylpropionylamino)-3-[cis-(2RS,3RS)-2-(hydroxymethyl)-tetrahydrofuran-3-yl]benzoate(Intermediate 32, 0.14 g) and triethylamine (0.15 mL) in DCM (5 mL) andthe resultant mixture was stirred at room temperature for 30 minutes.The mixture was washed with 1M hydrochloric acid, dried (MgSO₄) andfiltered. The filtrate was evaporated to dryness to give methyl2-acetylamino-6-(2,2-dimethylpropionylamino)-3-[cis-(2RS,3RS)-2-(methanesulfonyloxymethyl)-tetrahydrofuran-3-yl]benzoate(0.166 g) as a gum.

LCMS (Method B) r/t 2.57 (M+Na) 493.

Intermediate 32: Methyl2-acetylamino-6-(2,2-dimethylpropionylamino)-3-[cis-(2RS,3RS)-2-(hydroxymethyl)-tetrahydrofuran-3-yl]benzoate

A solution of methyl2-acetylamino-6-(2,2-dimethylpropionylamino)-3-(2-hydroxymethylfuran-3-yl)benzoate(Intermediate 38, 0.2 g) in dioxane (4 mL) and acetic acid (1 mL) wastreated under an atmosphere of nitrogen with palladium hydroxide oncarbon (10%, 0.03 g). The nitrogen was replaced by hydrogen and themixture was stirred under an atmosphere of hydrogen overnight. Themixture was filtered through Celite and the pad was washed thoroughlywith ethyl acetate. The filtrate was evaporated to dryness and theresidue was purified by chromatography on silica eluting with a mixtureof methanol and ethyl acetate with a gradient of 0-10% to give methyl2-acetylamino-6-(2,2-dimethylpropionylamino)-3-[cis-(2RS,3RS)-2-(hydroxymethyl)tetrahydrofuran-3-yl]benzoate(0.14 g) as a white solid.

¹H NMR (CDCl₃) δ: 9.70 (1H, br s), 8.29 (1H, d), 8.25 (1H, br s), 7.36(1H, d), 4.22 (1H, m), 4.10 (1H, m), 3.91 (1H, m), 3.90 (3H, s), 3.64(2H, m), 3.24 (1H, m), 2.41 (1H, m), 2.16 (3H, s), 2.11 (1H, m), 1.30(9H, s).

Intermediate 33: Methyl2-acetylamino-6-(2,2-dimethylpropionylamino)-3-(2-hydroxymethylfuran-3-yl)benzoate

Tetrabutylammonium fluoride (1M solution in THF, 1.1 mL) was added to astirred, cooled solution of methyl2-acetylamino-3-[2-(tert-butyldimethylsilanyloxymethyl)-furan-3-yl]-6-(2,2-dimethylpropionylamino)benzoate(Intermediate 34, 0.43 g) in THF (10 mL) at 0° C. and the mixture wasstirred at 0° C. for 40 minutes then evaporated to dryness. The residuewas partitioned between ethyl acetate and water and the organic layerwas washed with brine, dried (MgSO₄) and filtered. The filtrate wasevaporated to dryness and the residue was purified by chromatography onsilica eluting with a mixture of methanol and ethyl acetate with agradient of 0-2% to give methyl2-acetylamino-6-(2,2-dimethylpropionylamino)-3-(2-hydroxymethylfuran-3-yl)benzoate(0.2 g) as a gum.

¹H NMR (CDCl₃) δ: 9.95 (1H, br s), 8.36 (1H, d), 8.00 (1H, br s), 7.46(1H, s), 7.36 (1H, d), 6.32 (1H, s), 4.54 (2H, d), 3.90 (3H, s), 2.45(1H, t), 1.99 (3H, s), 1.32 (9H, s).

Intermediate 34: Methyl2-acetylamino-3-[2-(tert-butyldimethylsilanyloxymethyl)-furan-3-yl]-6-(2,2-dimethylpropionylamino)benzoate

Acetyl chloride (0.09 mL) was added to a stirred solution of methyl2-amino-3-[2-(tert-butyldimethylsilanyloxymethyl)furan-3-yl]-6-(2,2-dimethylpropionylamino)-benzoate(Intermediate 35, 0.47 g) in DCM (5 mL) and pyridine (0.16 mL) and themixture was stirred at room temperature for 1 hour. The mixture wasdiluted with DCM and washed with water and brine, dried (MgSO₄) andfiltered. The filtrate was evaporated to dryness and the residue waspurified by chromatography on silica eluting with a mixture of ethylacetate and cyclohexane with a gradient of 20-50% to give methyl2-acetylamino-3-[2-(tert-butyldimethylsilanyloxymethyl)-furan-3-yl]-6-(2,2-dimethylpropionylamino)benzoate(0.442 g) as a colourless foam.

¹H NMR (CDCl₃) δ: 10.08 (1H, br s), 8.34 (1H, d), 8.15 (1H, br s), 7.46(1H, s), 7.36 (1H, d), 6.32 (1H, s), 4.51 (2H, s), 3.93 (3H, s), 1.98(3H, s), 1.32 (9H, s), 0.93 (9H, s), 0.13 (6H, s).

Intermediate 35: Methyl2-amino-3-[2-(tert-butyldimethylsilanyloxymethyl)furan-3-yl]-6-(2,2-dimethylpropionylamino)-benzoate

Pivaloyl chloride (0.353 g) was added to a stirred, cooled mixture ofmethyl2,6-diamino-3-[2-(tert-butyldimethylsilanyloxymethyl)furan-3-yl]benzoate(Intermediate 36, 1.0 g) and sodium bicarbonate (0.268 g) in ethylacetate (20 mL) and water (7 mL) at 0° C. The mixture was allowed towarm to room temperature and stirred for 1.5 hours. Further pivaloylchloride (0.048 g) was added and the mixture was stirred for 1 hour.Ethyl acetate was added and the layers were separated. The organic layerwas washed with aqueous sodium bicarbonate solution dried (MgSO₄) andfiltered. The filtrate was evaporated to dryness and the residue waspurified by chromatography on silica eluting with a mixture of ethylacetate and cyclohexane with a gradient of 5-20% to give methyl2-amino-3-[2-(tert-butyldimethylsilanyloxymethyl)furan-3-yl]-6-(2,2-dimethylpropionylamino)benzoate(0.744 g) as an oil.

¹H NMR (CDCl₃) δ: 10.81 (1H, br s), 7.97 (1H, d), 7.48 (1H, s), 7.18(1H, d), 6.41 (1H, s), 5.67 (2H, s), 4.51 (2H, s), 3.98 (3H, s), 1.33(9H, s), 0.87 (9H, s), 0.05 (6H, s).

Intermediate 36: Methyl2,6-diamino-3-[2-(tert-butyldimethylsilanyloxymethyl)-furan-3-yl]benzoate

A mixture of methyl 3-bromo-2,6-diaminobenzoate (Intermediate 25, 2.6g), 2-(tert-butyldimethylsilanyloxymethyl)furan-3-boronic acid(Intermediate 37, 3.5 g), cesium carbonate (11.35 g),tri-tert-butylphosphonium tetrafluoroborate (0.334 g) andtris-(dibenzylideneacetone)dipalladium (0.529 g) in dioxane (72 mL) andwater (18 mL) was degassed and purged with nitrogen then heated at 70°C. for 75 minutes. After cooling, ethyl acetate and water were added andthe mixture was filtered through Celite. The filtrate was separated andthe organic layer was washed with brine, dried (MgSO₄) and filtered. Thefiltrate was evaporated to dryness and the residue was purified bychromatography on silica eluting with a mixture of ethyl acetate andcyclohexane with a gradient of 5-20% to give methyl2,6-diamino-3-[2-(tert-butyldimethylsilanyloxymethyl)furan-3-yl]benzoate(2.39 g) as a viscous oil which was used without furthercharacterization.

Intermediate 37: 2-(tert-Butyldimethylsilanyloxymethyl)furan-3-boronicacid

n-Butyllithium (2.5M in hexanes, 11.25 mL) was added slowly to astirred, cooled solution of3-bromo-2-(tert-butyldimethylsilanyloxymethyl)furan (Intermediate 38,7.5 g) in dry ether (150 mL) while maintaining the temperature below−70° C. The mixture was stirred at −78° C. for 2.5 hours. Tri-isopropylborate (6.75 g) was added and the mixture was allowed to warm to roomtemperature and stirred for 1.75 hours. Ethyl acetate and aqueousammonium chloride solution were added and the layers were separated. Theorganic layer was washed with aqueous ammonium chloride solution, dried(MgSO₄) and filtered. The filtrate was evaporated to dryness and theresidue was purified by chromatography on silica eluting with a mixtureof ethyl acetate and cyclohexane with a gradient of 10-35% to give2-(tert-butyldimethylsilanyloxymethyl)furan-3-boronic acid (3.6 g) whichwas used directly without further characterization.

Intermediate 38: 3-Bromo-2-(tert-butyldimethylsilanyloxymethyl)furan

tert-Butyldimethylsilanyl triflate (17.13 g) was added slowly to astirred, cooled solution of 3-bromo-2-hydroxymethylfuran (Intermediate39, 10.1 g) in DCM (160 mL) and pyridine (9.57 g) while maintaining thetemperature at 0° C. The mixture was allowed to warm to room temperatureand stirred for 1 hour. The mixture was washed with aqueous citric acidsolution, brine, dried (Na₂SO₄) and filtered. The filtrate wasevaporated to dryness to give3-bromo-2-(tert-butyldimethylsilanyloxymethyl)furan (17.1 g).

¹H NMR (CDCl₃) δ: 7.35 (1H, d), 6.38 (1H, d), 4.65 (2H, s), 0.90 (9H,s), 0.09 (6H, s).

Intermediate 39: 3-Bromo-2-hydroxymethylfuran

Sodium borohydride (1.14 g) was added slowly to a stirred, cooledsolution of 3-bromo-2-formylfuran (5 g) in a mixture of THF (50 mL) andmethanol (25 mL) while maintaining the temperature around 0° C. Themixture was allowed to warm to room temperature and stirred for 1 hour.The mixture was evaporated to dryness and the residue was partitionedbetween ethyl acetate and water. The aqueous layer was extracted withethyl acetate and the combined organic layers were washed with brine,dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness togive 3-bromo-2-hydroxymethylfuran (5.31 g) as a colourless oil.

¹H NMR (CDCl₃) δ: 7.37 (1H, d), 6.42 (1H, d), 4.65 (2H, d), 1.71 (1H,t).

Intermediate 40: Methyl(1aRS,7bSR)-5-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

A solution of methyl(1aRS,7bSR)-5-(2-bromo-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 41, 0.208 g) andN,N-diethyl-N—((Z)-1-tributylstannanylprop-1-en-3-yl)-amine(Intermediate 11, 0.367 g) in dioxane (5 mL) and DMSO (0.5 mL) wasde-gassed and flushed with nitrogen.Tris-(dibenzylideneacetone)-dipalladium (0.021 g) andtri-tert-butylphosphonium tetrafluoroborate (0.013 g) were added and themixture was again de-gassed and flushed with nitrogen. The resultantmixture was heated at 95° C. for 45 minutes. After cooling, the mixturewas partitioned between ethyl acetate and water and the organic layerwas dried (MgSO₄) and filtered. The filtrate was concentrated in vacuoand the residue was purified by chromatography on silica, eluting with amixture of methanol and DCM, with a gradient of 0-12% to give methyl(1aRS,7bSR)-5-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.188 g) as a yellow/brown oil.

¹H NMR (CDCl₃) δ: 8.06 (1H, dd), 7.16 (1H, d), 7.09-7.03 (2H, m), 6.94(1H, d), 6.86 (1H, d), 6.10-6.02 (1H, m), 4.33 (1H, d), 3.84 (3H, s),3.78 (1H, d), 3.13 (2H, br, d), 2.54 (4H, br, q), 1.88 (1H, m), 1.71(1H, m), 1.03-0.92 (8H, m).

Intermediate 41: Methyl(1aRS,7bSR)-5-(2-bromo-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Methyl(1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 42, 0.120 g) was suspended in DCM (5 mL). Pyridine (0.885mL) and 2-bromo-4-fluorobenzenesufonyl chloride (0.180 g) were added.The mixture was stirred at room temperature for 5 hours thenconcentrated in vacuo. The residue was dissolved in ethyl acetate andwashed with 0.5M aqueous hydrochloric acid solution, dried (MgSO₄) andfiltered. The filtrate was concentrated in vacuo and the residue waspurified by chromatography on silica, eluting with a mixture of ethylacetate and cyclohexane, with a gradient of 5-10% to give methyl(1aRS,7bSR)-5-(2-bromo-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.208 g) as a colourless oil.

¹H NMR (CDCl₃) δ: 9.31 (1H, br, s), 8.14 (1H, dd), 7.41 (1H, dd), 7.17(1H, d), 7.11 (1H, ddd), 7.06 (1H, d), 4.34 (1H, dd), 3.90 (3H, s), 3.80(1H, dd), 1.94-1.85 (1H, m), 1.75-1.67 (1H, m), 1.01 (2H, m).

Intermediate 42: Methyl(1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Methyl(1aRS,7bSR)-5-(2,2-dimethylpropionylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 43, 0.310 g) was suspended in methanol (7.5 mL) andconcentrated sulphuric acid (4 drops) was added. The reaction mixturewas heated to reflux, under an atmosphere of nitrogen, for 36 hours. Afurther 2 drops of concentrated sulphuric acid was added and heating wascontinued for a further 24 hours. After cooling, the mixture wasconcentrated in vacuo and the residue was partitioned between ethylacetate and saturated aqueous potassium carbonate solution. The aqueouslayer was extracted with ethyl acetate and the combined organic layerswere dried (Na₂SO₄) and filtered. The filtrate was concentrated in vacuoand the residue was purified by chromatography on silica, eluting with amixture of ethyl acetate and cyclohexane, with a gradient of 5-20% togive methyl(1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.120 g) as an off-white solid.

¹H NMR (CDCl₃) δ: 7.06 (1H, d), 6.26 (1H, d), 4.33 (1H, d), 3.87 (3H,s), 3.85 (1H, d), 1.83 (1H, td), 1.64 (1H, m), 0.99-0.89 (2H, m).

Intermediate 42A: Methyl(1aR,7bS)-5-amino-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Sample from Intermediate 42 was subjected to chiral SFC separation usinga Lux C-3 column, 50 mm×250 mm, particle size 5 micron. Eluting with 5%methanol (+0.1% diethylamine) in CO₂

Absolute configuration of Intermediate 42A was confirmed by conversionof a sample to Example 12 and comparison with the analytical chiralHPLC.

Intermediate 43: Methyl(1aRS,7bSR)-5-(2,2-dimethylpropionylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Methyl(1aRS,7bSR)-1,1-dibromo-5-(2,2-dimethylpropionylamino)-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate(Intermediate 44, 1.13 g) was suspended in ethanol (30 mL). Zinc dust(1.17 g), followed by ammonium chloride (1.31 g) were added and thereaction mixture was heated to reflux, under an atmosphere of nitrogen,for 6 hours. After cooling, the solid was filtered off and washed withethyl acetate. The filtrate was concentrated in vacuo and the residuewas purified by chromatography on silica, eluting with a mixture ofether and cyclohexane, with a gradient of 5-12.5% to give methyl(1aRS,7bSR)-5-(2,2-dimethylpropionylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.310 g) as a colourless oil.

¹H NMR (CDCl₃) δ: 9.72 (1H, br, s), 7.98 (1H, d), 7.30 (1H, d), 4.36(1H, dd), 3.91 (3H, s), 3.84 (1H, dd), 1.95 (1H, td), 1.73 (1H, m), 1.28(9H, s), 1.03 (2H, m).

Intermediate 44: Methyl(1aRS,7bSR)-1,1-dibromo-5-(2,2-dimethylpropionylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Methyl 7-(2,2-dimethylpropionylamino)-2H-chromene-8-carboxylate(Intermediate 45, 2.372 g) and benzyl triethyl ammonium chloride (0.373g) were suspended in bromoform (6.45 mL) and aqueous sodium hydroxidesolution (50%, 3.64 mL) was added dropwise. The resultant blacksuspension was heated to 60° C. for 2 hours. After cooling, the mixturewas partitioned between water and ethyl acetate. The emulsion formed wasfiltered through a pad of Celite and the organic layer was decanted off.The aqueous was re-extracted with ethyl acetate and the combined organiclayers were dried (MgSO₄) and filtered. The filtrate was concentrated invacuo and the residue was purified by chromatography on silica, elutingwith a mixture of ethyl acetate and cyclohexane, with a gradient of2.5-15% to give methyl1,1-dibromo-5-(2,2-dimethylpropionylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(1.557 g) as an off-white solid.

¹H NMR (CDCl₃) δ: 9.89 (1H, br, s), 8.13 (1H, d), 7.43 (1H, d), 4.47(1H, dd), 4.32 (1H, dd), 3.91 (3H, s), 2.89 (1H, d), 2.45 (1H, ddd),1.30 (9H, s).

Intermediate 45: Methyl7-(2,2-dimethylpropionylamino)-2H-chromene-8-carboxylate

A solution of methyl2-(2,2-dimethylpropionylamino)-6-(prop-2-ynyloxy)benzoate (Intermediate46, 4.74 g) and[bis(trifluoromethanesulfonyl)imidate]-(triphenylphosphine)gold (2:1)toluene adduct (0.060 g) in toluene (70 mL) was heated to 85° C., underan atmosphere of nitrogen for 3 hours. After cooling, the mixture wasconcentrated in vacuo and the residue was purified by chromatography onsilica, eluting with a mixture of ethyl acetate and cyclohexane, with agradient of 0-20% to give methyl7-(2,2-dimethylpropionylamino)-2H-chromene-8-carboxylate (3.59 g) as acolourless oil.

¹H NMR (CDCl₃) δ: 10.02 (1H, br, s), 8.05 (1H, d), 7.05 (1H, d), 6.39(1H, ddd), 5.76 (1H, dt), 4.83 (2H, dd), 3.93 (3H, s), 1.30 (9H, s).

Intermediate 46: Methyl2-(2,2-dimethylpropionylamino)-6-(prop-2-ynyloxy)benzoate

A mixture of methyl 2-(2,2-dimethylpropionylamino)-6-hydoxybenzoate(Intermediate 47, 4.57 g), propargyl bromide (80% solution in toluene,2.03 mL) and potassium carbonate (3.74 g) in acetone (35 mL) was heatedat reflux for 8 hours. After cooling, the mixture was filtered and thefiltrate was concentrated in vacuo. The residue was purified bychromatography on silica, eluting with a mixture of ethyl acetate andcyclohexane, with a gradient of 5-20% to give methyl2-(2,2-dimethylpropionylamino)-6-(prop-2-ynyloxy)benzoate (4.74 g) as anoil which crystallised on standing to give a white solid.

¹H NMR (CDCl₃) δ: 9.89 (1H, br, s), 8.16 (1H, dd), 7.41 (1H, t), 6.83(1H, dd), 4.74 (2H, d), 3.95 (3H, s), 2.53 (1H, t), 1.31 (9H, s).

Intermediate 47: Methyl 2-(2,2-dimethylpropionylamino)-6-hydroxybenzoate

Trimethylacetyl chloride (3.69 g) was added to a mixture of methyl2-amino-6-hydroxybenzoate (prepared according to Comess et al, US20040167128, 3.99 g) and sodium bicarbonate (2.57 g) in ethyl acetate (77mL) and water (18 mL). The reaction mixture was stirred at roomtemperature for 1 hour. A further amount of trimethylacetyl chloride(1.85 g) was added and the mixture was stirred for 1 hour. A furtheramount of trimethylacetyl chloride (0.920 g) was added and the mixturewas stirred for 30 minutes. The mixture was diluted with ethyl acetate,the layers were separated and the organic layer was dried (Na₂SO₄) andfiltered. The filtrate was concentrated in vacuo and the residue waspurified by chromatography on silica, eluting with a mixture of ethylacetate and cyclohexane, with a gradient of 5-25% to give methyl2-(2,2-dimethylpropionylamino)-6-hydroxybenzoate (5.79 g) as a whitesolid.

¹H NMR (CDCl₃) δ: 10.32 (1H, br, s), 8.22 (1H, dd), 7.41 (1H, t), 6.71(1H, dd), 4.08 (3H, s), 1.33 (9H, s).

Intermediate 48: Methyl(1aRS,7bSR)-5-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-7b-methyl-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 40, startingfrom methyl(1aRS,7bSR)-5-(2-bromo-4-fluorobenzenesulfonylamino)-7b-methyl-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 49) andN,N-diethyl-N—((Z)-1-tributylstannanylprop-1-en-3-yl)amine (Intermediate11).

¹H NMR (CDCl₃) δ: 8.07 (1H, dd), 7.28 (1H, d), 7.05 (2H, m), 6.95 (1H,d), 6.88 (1H, d), 6.06 (1H, m), 4.28 (1H, d), 3.85 (3H, s), 3.83 (1H,d), 3.14 (2H, br d), 2.53 (4H, q), 1.41 (3H, s), 1.12 (1H, m), 1.07 (1H,t), 0.93 (6H, t), 0.84 (1H, dd).

Intermediate 49: Methyl(1aRS,7bSR)-5-(2-bromo-4-fluorobenzenesulfonylamino)-7b-methyl-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 41, startingfrom methyl(1aRS,7bSR)-5-amino-7b-methyl-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 50) and 2-bromo-4-fluorobenzenesulfonyl chloride.

¹H NMR (CDCl₃) δ: 9.18 (1H, br s), 8.14 (1H, dd), 7.41 (1H, dd), 7.29(1H, d), 7.11 (1H, m), 7.08 (1H, d), 4.28 (1H, d), 3.89 (3H, s), 3.84(1H, d), 1.44 (1H, m), 1.42 (3H, s), 1.10 (1H, t), 0.83 (1H, dd).

Intermediate 50: Methyl(1aRS,7bSR)-5-amino-7b-methyl-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

Trifluoroacetic acid (4 mL) was added to a solution of methyl(1aRS,7bSR)-5-(tert-butoxycarbonylamino)-7b-methyl-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(Intermediate 51, 0.6 g) in dichloromethane (4 mL) and the resultantdark solution was stirred at room temperature for 1 hour. The solutionwas evaporated to dryness and the residue was partitioned between waterand ethyl acetate and treated with a small amount of solid sodiumbicarbonate until the pH of the aqueous layer was >7. The layers wereseparated and the aqueous layer was extracted with ethyl acetate. Thecombined organic layers were washed with water, dried (MgSO₄) andfiltered. The filtrate was evaporated to dryness to give methyl(1aRS,7bSR)-5-amino-7b-methyl-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(0.402 g) as a red/orange solid.

¹H NMR (CDCl₃) δ: 7.20 (1H, d), 6.30 (1H, d), 4.27 (1H, d), 3.90 (1H,d), 3.88 (3H, s), 1.42 (3H, s), 1.37 (1H, m), 1.06 (1H, t), 0.78 (1H,dd).

Intermediate 51: Methyl(1aRS,7bSR)-5-(tert-butoxycarbonylamino)-7b-methyl-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 43, startingfrom methyl(1aRS,7bSR)-5-(tert-butoxycarbonylamino)-1,1-dibromo-7b-methyl-1,1a,2,7b-tetrahydro-cyclopropa-[c]chromene-4-carboxylate(Intermediate 52).

¹H NMR (CDCl₃) δ: 8.27 (1H, br s), 7.72 (1H, d), 7.38 (1H, d), 4.29 (1H,d), 3.91 (3H, s), 3.88 (1H, d), 1.50 (9H, s), 1.46 (3H, s), 1.44 (1H,m), 1.13 (1H, t), 0.84 (1H, dd).

Intermediate 52: Methyl(1aRS,7bSR)-1,1-dibromo-5-(tert-butoxycarbonylamino)-7b-methyl-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 44, startingfrom methyl4-methyl-7-(tert-butoxycarbonylamino)-2H-chromene-8-carboxylate(Intermediate 53).

¹H NMR (CDCl₃) δ: 8.55 (1H, br s), 7.87 (1H, d), 7.42 (1H, d), 4.75 (1H,dd), 4.13 (1H, dd), 3.92 (3H, s), 2.05 (1H, dd), 1.79 (3H, s), 1.50 (9H,s).

Intermediate 53: Methyl4-methyl-7-(tert-butoxycarbonylamino)-2H-chromene-8-carboxylate

Prepared by proceeding in a similar manner to Intermediate 45, startingfrom methyl2-[bis-(tert-butyoxycarbonyl)amino]-6-(but-2-ynyloxy)benzoate(Intermediate 54).

¹H NMR (CDCl₃) δ: 8.66 (1H, br s), 7.77 (1H, d), 7.18 (1H, dd), 5.53(1H, m), 4.73 (2H, m), 3.93 (3H, s), 1.99 (3H, q), 1.51 (9H, s).

Intermediate 54: Methyl2-[bis-(tert-butyoxycarbonyl)amino]-6-(but-2-ynyloxy)benzoate

Prepared by proceeding in a similar manner to Intermediate 46, startingfrom methyl 2-[bis-(tert-butyoxycarbonyl)amino]-6-hydroxybenzoate(Intermediate 55) and 1-bromobut-2-yne

¹H NMR (CDCl₃) δ: 7.36 (1H, t), 7.08 (1H, dd), 6.82 (1H, dd), 4.70 (2H,q), 3.84 (3H, s), 1.84 (3H, t), 1.39 (18H, s).

Intermediate 55: Methyl2-[bis-(tert-butyoxycarbonyl)amino]-6-hydroxybenzoate

Prepared by proceeding in a similar manner to Intermediate 4, startingfrom methyl2-[bis-(tert-butoxycarbonyl)amino]-6-(4-methylbenzenesulfonyloxy)benzoate(Intermediate 56)

¹H NMR (CDCl₃) δ: 11.17 (1H, s), 7.40 (1H, t), 6.99 (1H, dd), 6.69 (1H,dd), 3.92 (3H, s), 1.37 (18H, s).

Intermediate 56: Methyl2-[bis-(tert-butoxycarbonyl)amino]-6-(4-methylbenzenesulfonyloxy)-benzoate

Prepared by proceeding in a similar manner to Intermediate 6, startingfrom methyl 2-amino-6-hydroxybenzoate (prepared according to Comess etal, US2004 0167128)

¹H NMR (CDCl₃) δ: 7.72 (2H, d), 7.40 (1H, t), 7.31 (2H, d), 7.22 (1H,dd), 7.11 (1H, dd), 3.71 (3H, s), 2.44 (3H, s), 1.33 (18H, s).

Intermediate 57:Cis-(3aRS,9bRS)-7-(2-fluorobenzenesulfonylamino)-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylicacid

A mixture of lithium hydroxide (0.5 g) and methylcis-(3aRS,9bRS)-7-(2-fluorobenzenesulfonyl-amino)-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate(Intermediate 58, 0.217 g) in a mixture of dioxane (13 mL) and water (4mL) was divided between two microwave vials and the mixtures wereirradiated in the microwave at 150° C. for 10 minutes. After cooling,the combined mixture was acidified by addition of 10% aqueous citricacid (2 mL), extracted with DCM, dried (MgSO₄) and filtered. Thefiltrate was evaporated to dryness to givecis-(3aRS,9bRS)-7-(2-fluorobenzenesulfonylamino)-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylicacid (0.518 g) as a glass.

¹H NMR (CDCl₃) δ: 12.00 (1H, br s), 11.57 (1H, br s), 7.97 (1H, dt),7.55 (1H, m), 7.43 (1H, d), 7.26 (2H, m), 7.15 (1H, t), 4.43 (1H, dd),4.37 (1H, m), 4.14 (1H, dd), 3.83 (2H, m), 3.50 (1H, m), 2.50 (1H, m),1.87 (1H, m).

Intermediate 58: Methylcis-(3aRS,9bRS)-7-(2-fluorobenzenesulfonylamino)-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate

2-Fluorobenzenesulfonyl chloride (0.5 g) was added to a solution ofmethylcis-(3aRS,9bRS)-7-amino-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate(Intermediate 19, 0.53 g) in DCM (10 mL) and pyridine (20 mL) and theresultant mixture was stirred at room temperature for 48 hours. Themixture was evaporated to dryness and the residue was treated withwater, extracted with DCM, dried (MgSO₄) and filtered. The filtrate wasevaporated to dryness and the residue was purified by chromatography onsilica, eluting with a mixture of ethyl acetate and cyclohexane with agradient of 0-60% to give methylcis-(3aRS,9bRS)-7-(2-fluorobenzenesulfonylamino)-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylate(0.574 g) as a pale yellow solid.

¹H NMR (CDCl₃) δ: 9.11 (1H, s), 7.85 (1H, dt), 7.53 (1H, m), 7.23 (1H,d), 7.21 (1H, dt), 7.15 (1H, d), 7.13 (1H, dd), 4.28 (1H, m), 4.04 (1H,dd), 3.95 (1H, dd), 3.87 (3H, s), 3.82 (2H, m), 3.41 (1H, m), 2.45 (1H,m), 1.84 (1H, m).

Intermediate 59: Methyl(1aRS,7bSR)-5-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,1-difluoro-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 9, startingfrom methyl(1aRS,7bSR)-5-(2-bromo-4-fluorobenzenesulfonylamino)-1,1-difluoro-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate(Intermediate 60) andN,N-diethyl-N—((Z)-1-tributylstannanylprop-1-en-3-yl)amine (Intermediate11) as a pale yellow gum.

¹H NMR (CDCl₃) δ: 8.11 (1H, dd), 7.18 (1H, d), 7.13-7.04 (2H, m), 6.98(1H, d), 6.93 (1H, d), 6.08 (1H, m), 4.38 (1H, d), 4.02 (1H, m), 3.87(3H, s), 3.23-3.04 (2H, br s), 2.67 (1H, t), 2.60-2.43 (4H, br s), 3.32(1H, m), 0.94 (6H, t).

Intermediate 60: Methyl(1aRS,7bSR)-5-(2-bromo-4-fluorobenzenesulfonylamino)-1,1-difluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 18, startingfrom methyl(1aRS,7bSR)-5-amino-1,1-difluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 61) and 2-bromo-4-fluorobenzene sulfonyl chloride, as acolourless foam.

¹H NMR (CDCl₃) δ: 9.58 (1H, s), 8.18 (1H, dd), 7.42 (1H, dd), 7.20 (1H,d), 7.13 (1H, d), 7.16-7.08 (1H, m), 4.38 (1H, d), 4.03 (1H, m), 3.91(3H, s), 2.67 (1H, t), 2.32 (1H, m).

Intermediate 61: Methyl(1aRS,7bSR)-5-amino-1,1-difluoro-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 42, startingfrom methyl(1aRS,7bSR)-5-(2,2-dimethylpropionylamino)-1,1-difluoro-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate(Intermediate 62) as an off white solid.

¹H NMR (CDCl₃) δ: 7.07 (1H, d), 6.30 (1H, d), 5.19-4.95 (2H, br s), 4.32(1H, d), 4.11 (1H, m), 3.87 (3H, s), 2.60 (1H, t), 2.27 (1H, m).

Intermediate 62: Methyl(1aRS,7bSR)-5-(2,2-dimethylpropionylamino)-1,1-difluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Methyl 7-(2,2-dimethylpropionylamino)-2H-chromene-8-carboxylate(Intermediate 45, 1.0 g) was dissolved in diglyme (30 mL) and thesolution was heated to 160° C. Sodium chlorodifluoroacetate (4.27 g) wasadded in portions over 15 minutes with the final portion being washed inwith diglyme (15 mL). On completion of the addition the mixture washeated at 180° C. for 15 minutes. After cooling, the mixture was pouredinto water and extracted with ethyl acetate, washed with water, dried(MgSO₄) and filtered. The filtrate was evaporated to dryness and theresidue was purified by chromatography on silica, eluting with a mixtureof ethyl acetate and pentane with a gradient of 2.5-15% to give methyl(1aRS,7bSR)-5-(2,2-dimethylpropionylamino)-1,1-difluoro-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate(0.66 g) as a colourless oil.

¹NMR (CDCl₃) δ: 9.86 (1H, br s), 8.12 (1H, d), 7.33 (1H, d), 4.41 (1H,d), 4.07 (1H, m), 3.92 (3H, s), 2.74 (1H, t), 2.34 (1H, m), 1.29 (9H,s).

Intermediate 63: Methyl(1aRS,7bSR)-5-[2-((Z)-3-ethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Methane sulfonic anhydride (0.09 g) was added to a stirred, cooledmixture of methyl(1aRS,7bSR)-5-{N-[methoxycarbonyl]-N-[2-((Z)-3-hydroxyprop-1-enyl)-4-fluorobenzenesulfonyl]amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 64, 0.17 g) and N,N-di-isopropyl-N-ethylamine (0.134 g) inDCM (10 mL) at 0° C. The temperature was allowed to rise to roomtemperature and the mixture was stirred for 2 hours. A solution ofethylamine (2M in toluene, 2 mL) was added and the resultant mixture wasstirred at room temperature for 3 hours then diluted with water. Theorganic layer was separated, dried (Na₂SO₄) and filtered. The filtratewas evaporated to dryness to give methyl(1aRS,7bSR)-5-[2((Z)-3-ethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate(0.09 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.89 (1H, dd), 7.35 (1H, d), 7.16 (1H, m), 7.08 (1H,d), 6.83 (1H, d), 6.58 (1H, d), 5.69 (1H, m), 4.17 (1H, d), 3.84-3.04(2H, br s), 3.67 (3H, s), 3.58 (1H, d), 2.78 (2H, m), 1.83 (1H, m), 1.66(1H, m), 1.04 (3H, t), 0.88 (1H, m), 0.64 (1H, m).

Intermediate 64: Methyl(1aRS,7bSR)-5-{N-[2-((Z)-3-hydroxyprop-1-enyl)-4-fluorobenzene-sulfonyl]-N-[methoxycarbonyl]amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

A mixture of methyl(1aRS,7bSR)-5-[N-(2-bromo-4-fluorobenzenesulfonyl)-N-(methoxycarbonyl)amino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(Intermediate 65, 0.6 g), (Z)-3-tributylstannanylprop-2-en-1-ol(Intermediate 12, 0.81 g), tris-(dibenzylideneacetone)dipalladium (0.1g) and tri-tert-butylphosphonium tetrafluoroborate (0.07 g) in dioxane(18 mL) and DMSO (2 mL) was stirred at room temperature for 30 minutes.The resultant mixture was diluted with ethyl acetate and washed withwater, dried (Na₂SO₄) and filtered. The filtrate was evaporated todryness and the residue was purified by chromatography on silica,eluting with a mixture of ethyl acetate and petroleum ether with agradient of 30-50% to give methyl(1aRS,7bSR)-5-{N-[2-((Z)-3-hydroxyprop-1-enyl)-4-fluorobenzenesulfonyl]-N-[methoxycarbonyl]amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(0.55 g) as an off-white solid.

¹H NMR (CDCl₃) δ: 8.19 (1H, m), 7.39 (1H, d), 7.16 (1H, m), 7.02 (1H,m), 6.96 (2H, m), 6.03 (1H, m), 4.41 (1H, m), 4.23 (2H, m), 3.88 (1H,dd), 3.71 (3H, 2s), 3.65 (3H, 2s), 2.06 (1H, m), 1.82 (1H, m), 1.25 (1H,m), 1.14 (1H, m).

Intermediate 65: Methyl(1aRS,7bSR)-5-[N-(2-bromo-4-fluorobenzenesulfonyl)-N-(methoxycarbonyl)amino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

A solution of methyl(1aRS,7bSR)-5-(2-bromo-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 41, 1.7 g) in THF (20 mL) was added to a suspension ofsodium hydride (70% oil dispersion, 0.2 g) in THF (10 mL). The resultantsolution was stirred for 30 minutes then methyl chloroformate (0.53 g)was added. The resultant mixture was stirred at room temperatureovernight. Saturated aqueous sodium bicarbonate was added and themixture was extracted with ethyl acetate, dried (Na₂SO₄) and filtered.The filtrate was evaporated to dryness and the residue was purified bychromatography on silica, eluting with a mixture of ethyl acetate andpetroleum ether (30%) to give methyl(1aRS,7bSR)-5-[N-(2-bromo-4-fluorobenzenesulfonyl)-N-(methoxycarbonyl)amino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(1.6 g) as a white solid.

¹H NMR (CDCl₃) δ: 8.42 (1H, m), 7.48 (1H, dd), 7.37 (1H, d), 7.19 (2H,m), 4.42 (1H, m), 3.95 (1H, dd), 3.86 (3H, s,), 3.69 (3H, s), 2.06 (1H,m), 1.84 (1H, m), 1.16 (2H, m).

Intermediate 66: Methyl(1aRS,7bSR)-5-{2[(Z)-3-(pyrrolidin-1-yl)prop-1-enyl]-4-fluorobenzenesulfonylamino)}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 63, startingfrom methyl(1aRS,7bSR)-5-{N-[methoxycarbonyl]-N-[2-((Z)-3-hydroxyprop-1-enyl)-4-fluorobenzenesulfonyl]amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 64) and pyrrolidine as a brown oil.

LCMS (Method D) r/t 1.28 (M+H) 487

Intermediate 67:(1aRS,7bSR)-5-(2-Fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylicacid

A mixture of methyl(1aRS,7bSR)-5-(2-Fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 68, 0.6 g) and lithium hydroxide monohydrate (1.5 g) indioxane (45 mL) and water (13.8 mL) was stirred and heated at 100° C.overnight. After cooling, the mixture was concentrated under vacuum andthe residue was diluted with water and acidified to pH3 with 1Mhydrochloric acid. The precipitated solid was collected by filtration togive(1aRS,7bSR)-5-(2-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.58 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 13.05 (1H, br s), 9.96 (1H, s), 7.73 (2H, m),7.45-7.31 (2H, m), 7.23 (1H, d), 6.64 (1H, d), 4.29 (1H, d), 3.74 (1H,d), 2.01 (1H, m), 1.80 (1H, m), 1.02 (1H, m), 0.81 (1H, m).

Intermediate 68: Methyl(1aRS,7bSR)-5-(2-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 41, startingfrom methyl(1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 42) and 2-fluorobenzenesulfonyl chloride.

¹H NMR (CDCl₃) δ: 8.90 (1H, s), 7.84 (1H, dt), 7.53 (1H, m), 7.24-7.11(4H, m), 4.34 (1H, d), 3.88 (3H, s), 3.80 (1H, dd), 1.91 (1H, m), 1.74(1H, m), 1.02 (2H, m).

Intermediate 69: Methyl(1aRS,7bSR)-5-{2[(Z)-3-(propan-2-yl)aminoprop-1-enyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 63, startingfrom methyl(1aRS,7bSR)-5-{N-[methoxycarbonyl]-N-[2-((Z)-3-hydroxyprop-1-enyl)-4-fluorobenzene-sulfonyl]amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 64) and 2-aminopropane.

LCMS (Method D) r/t 1.17 (M+H) 475.

Intermediate 70: Methyl(1aRS,7bSR)-5-{2[(Z)-3-((S)-3-hydroxypyrrolidin-1-yl)aminoprop-1-enyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 63, startingfrom methyl(1aRS,7bSR)-5-{N-[methoxycarbonyl]-N-[2-((Z)-3-hydroxyprop-1-enyl)-4-fluorobenzene-sulfonyl]amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 64) and (S)-3-hydroxypyrrolidine.

LCMS (Method D) r/t 1.14 (M+H) 503.

Intermediate 71: Methyl(1aRS,7bSR)-5-{2[(Z)-3-((R)-3-hydroxypyrrolidin-1-yl)aminoprop-1-enyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydro1 cyclopropa[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 63, startingfrom methyl(1aRS,7bSR)-5-{N-[methoxycarbonyl]-N-[2-((Z)-3-hydroxyprop-1-enyl)-4-fluorobenzene-sulfonyl]amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 64) and (R)-3-hydroxypyrrolidine and used without furthercharacterisation.

Intermediate 72: Methyl(1aRS,7bSR)-5-{N-(methoxycarbonyl)-N-[2((Z)-4-diethylaminobut-1-enyl)-4-fluorobenzenesulfonyl]amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Methyl sulfonic anhydride (0.062 g) was added to a stirred, cooledmixture of methyl(1aRS,7bSR)-5-{N-[methoxycarbonyl]-N-[2-((Z)-4-hydroxybut-1-enyl)-4-fluorobenzene-sulfonyl]amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 73, 0.12 g) and N,N-di-isopropyl-N-ethylamine (0.046 g) inDCM (15 mL) at 0° C. The resultant mixture was stirred at 0° C. for 20minutes. Diethylamine (0.026 g) was added and the mixture was thenstirred at room temperature for 24 hours. The mixture was diluted withwater and extracted with DCM, dried (Na₂SO₄) and filtered. The filtratewas evaporated to dryness and the residue was purified by chromatographyon silica, eluting with a mixture of methanol and DCM with a gradient of2-10% to give methyl(1aRS,7bSR)-5-{N-(methoxycarbonyl)-N-[2((Z)-4-diethylaminobut-1-enyl)-4-fluorobenzenesulfonyl]amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(0.08 g) as alight yellow solid.

LCMS (Method D) r/t 1.22 (M+H) 561.

Intermediate 73: Methyl(1aRS,7bSR)-5-{N-[methoxycarbonyl]-N-[2-((Z)-4-hydroxybut-1-enyl)-4-fluorobenzenesulfonyl]amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 64, startingfrom methyl(1aRS,7bSR)-5-[N-(2-bromo-4-fluorobenzenesulfonyl)-N-(methoxycarbonyl)amino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(Intermediate 65) and (Z)-4-tributylstannanylprop-3-en-1-ol (preparedaccording to Miura et al, Organic Letters, 2005, 7(3) 503).

¹H NMR (CDCl₃) δ: 8.18 (1H, m), 7.38 (1H, d), 7.13 (3H, m), 6.96 (1H,d), 5.91 (1H, m), 4.44 (1H, m), 3.98 (1H, dd), 3.79 (3H, s), 3.75 (2H,m), 3.65 (3H, s), 2.49 (2H, m), 2.07 (1H, m), 1.81 (1H, m), 1.27 (1H,m), 1.15 (1H, m).

Intermediate 74:(1aRS,7bSR)-5-(4-Fluoro-2-vinylbenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

Lithium hydroxide (0.101 g) was added to a solution of methyl(1aRS,7bSR)-5-(4-fluoro-2-vinylbenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 75, 0.150 g) in a mixture of dioxane (3 mL) and water (0.6mL) and the mixture was irradiated in the microwave at 130° C. for 30minutes. After cooling, the mixture evaporated to dryness and theresidue was acidified by addition of 10% aqueous citric acid (2 mL),extracted with DCM, dried (MgSO₄) and filtered. The filtrate wasevaporated to dryness and the residue was purified by chromatography onsilica eluting with a mixture of methanol and DCM with a gradient of0-10% to give(1aRS,7bSR)-5-(4-fluoro-2-vinylbenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid (0.0.35 g) as a glass.

¹H NMR (CDCl₃) δ: 11.69 (1H, br s), 8.10 (1H, dd), 7.50 (1H, dd),7.31-7.17 (3H, m), 7.03 (1H, dt), 5.60 (1H, d), 5.50 (1H, d), 4.60 (1H,d), 4.04 (1H, d), 1.97 (1H, m), 1.81 (1H, m), 1.20 (1H, m), 0.99 (1H,m).

Intermediate 75: Methyl(1aRS,7bSR)-5-(4-fluoro-2-vinylbenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

A mixture of methyl(1aRS,7bSR)-5-(2-bromo-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 41, 0.1 g), vinyl boronic acid pinacol ester (0.073 g),bis(triphenylphospine)palladium (II) chloride (0.034 g) and cesiumcarbonate (0.215 g) in dioxane (5 mL) and water (1 ml) was degassed andpurged with argon then irradiated in a microwave at 130° C. for 20minutes. After cooling, the mixture was partitioned between 1Mhydrochloric acid and ethyl acetate. The organic layer was dried (MgSO₄)and filtered and the filtrate evaporated to dryness to give methyl(1aRS,7bSR)-5-(4-fluoro-2-vinylbenzenesulfonyl-amino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.15 g) as a yellow glass.

¹H NMR (CDCl₃) δ: 8.99 (1H, br s), 7.97 (1H, dd), 7.38 (1H, dd), 7.21(1H, dd), 7.18 (1H, d), 7.05 (1H, d), 7.00 (1H, m), 5.59 (1H, d), 5.38(1H, d), 4.32 (1H, d), 3.77 (4H, m), 1.90 (1H, dt), 1.71 (1H, m), 1.00(2H, m).

Intermediate 76: Methyl(1aRS,7bSR)-5-{2-[(Z)-3-(azetidin-1-yl)prop-1-enyl]-4-fluoro-benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 63, startingfrom methyl(1aRS,7bSR)-5-{N-[methoxycarbonyl]-N-[2-((Z)-3-hydroxyprop-1-enyl)-4-fluorobenzene-sulfonyl]amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 64) and azetidine as a yellow oil.

LCMS (Method D) r/t 1.17 (M+H) 473.

Intermediate 77: Methyl(1aRS,7bSR)-5-{2-[(Z)-3-(3-hydroxyazetidin-1-yl)prop-1-enyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 63, startingfrom methyl(1aRS,7bSR)-5-{N-[methoxycarbonyl]-N-[2-((Z)-3-hydroxyprop-1-enyl)-4-fluorobenzene-sulfonyl]amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 64) and 3-hydroxyazetidine as a yellow oil.

LCMS (Method D) r/t 1.15 (M+H) 489.

Intermediate 78: N-(4-Dimethylaminobutyl)-N-methylamine

A solution of lithium aluminium hydride in THF (1M, 28 mL) was addeddropwise to a stirred, cooled solution ofN-(4-dimethylaminobutyl)formamide (Intermediate 79, 2.7 g) in THF (60mL) while maintaining the temperature at 0° C. under an atmosphere ofnitrogen. On completion of the addition, the mixture was stirred andheated at 75° C. for 2 hours. The reaction mixture was cooled to 0° C.and ethanol was added then the mixture was evaporated to dryness. Theresidue was diluted with a mixture of diethyl ether and DCM (30%) andthe solid was filtered off. The filtrate was evaporated to dryness togive N-(4-dimethylaminobutyl)-N-methylamine (1.5 g) as a yellow oil.

¹H NMR (CDCl₃) δ: 2.56 (2H, m), 2.41 (3H, s), 2.25 (2H, m), 2.20 (6H,s), 1.47 (4H, m).

Intermediate 79: N-(4-Dimethylaminobutyl)formamide

A solution of 4-dimethylaminobutylamine (3.0 g) in ethyl formate (30 mL)was stirred and heated at reflux under an atmosphere of nitrogen for 3hours. After cooling, the mixture was evaporated to dryness and theresidue was purified by chromatography on silica, eluting with a mixtureof methanol and DCM (20%) to give N-(4-dimethylaminobutyl)formamide (2.7g) as a pale yellow oil.

¹H NMR (CDCl₃) δ: 8.14 (1H, s), 6.80 (1H, s), 3.50 (2H, m), 2.28 (2H,m), 2.20 (6H, s), 1.61 (4H, m).

Intermediate 80: Methyl(1aRS,7bSR)-5-{2-[((S)-1-ethylpyrrolidin-3-ylcarbamoyl)methyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

A solution of methyl(1aRS,7bSR)-5-(2-carboxymethyl-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 83, 0.180 g), (S)-1-ethylpyrrolidin-3-ylamineditrifluoroacetic acid salt (Intermediate 81, 0.171 g), EDAC (0.144 g)and triethylamine (0.202 g) in DCM (5 mL) was allowed to stand at roomtemperature for 6 days then washed with water and filtered through aphase separator. The filtrate was directly purified by chromatography onsilica, eluting with a mixture of methanol and DCM with a gradient of0-20% to give methyl(1aRS,7bSR)-5-{2-[((S)-1-ethylpyrrolidin-3-ylcarbamoyl)methyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.178 g) as an off-white foam.

LCMS (Method E) r/t 2.57 (M+H) 532

Intermediate 81: (S)-1-Ethylpyrrolidin-3-ylamine ditrifluoroacetic acidsalt

A solution of tert-butyl ((S)-1-ethylpyrrolidin-3-yl)carbamate(Intermediate 82, 0.107 g) in a solution of trifluoroacetic acid (2 mL)and DCM (2 mL) was left to stand at room temperature for 30 minutes thenconcentrated in vacuo. The residue was azeotroped with toluene to give(S)-1-ethylpyrrolidin-3-ylamine ditrifluoroacetic acid salt (0.231 g) asa light brown gum which was used without further characterisation.

Intermediate 82: tert-Butyl ((S)-1-ethylpyrrolidin-3-yl)carbamate

A mixture of tert butyl (S)-pyrrolidin-3-ylcarbamate (1.048 g),iodoethane (0.90 g) and potassium carbonate (1.55 g) in acetonitrile (15mL) was stirred at room temperature for 17 hours then filtered. Thefiltrate was concentrated in vacuo and the residue was triturated withDCM and filtered. The filtrate was concentrated in vacuo and the residuewas purified by chromatography on silica, eluting with a mixture ofmethanol and DCM with a gradient of 0-35% to give tert-butyl((S)-1-ethylpyrrolidin-3-yl)carbamate (0.891 g) as a light coloured gum.

¹H NMR (CDCl₃) δ: 5.11 (1H, br, s), 4.29 (1H, br, s), 3.88 (1H, br, s),3.18 (1H, br, s), 2.90 (2H, br, m), 2.76 (2H, br, m), 2.62 (1H, br, q),2.38 (1H, m), 1.44 (9H, s), 1.28 (3H, t).

Intermediate 83: Methyl(1aRS,7bSR)-5-(2-carboxymethyl-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

1M Sodium hydroxide solution (3 mL) was added to a solution of methyl(1aRS,7bSR)-5-(4-fluoro-2-methoxycarbonylmethylbenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(Intermediate 84, 0.438 g) in methanol (6 mL) and the mixture was heatedat 50° C. for 2 hours. After cooling, the mixture was evaporated todryness and the residue was dissolved in ethyl acetate and water andacidified with concentrated hydrochloric acid. The organic layer wasdried (Na₂SO₄) and filtered and the filtrate was concentrated in vacuo,the residue was dissolved in touene and re-evaporated to give methyl(1aRS,7bSR)-5-(2-carboxymethyl-4-fluorobenzene-sulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.422 g) as a white solid.

¹H NMR (CDCl₃) δ: 8.83 (1H, br, s), 7.86 (1H, dd), 7.22 (1H, d), 7.01(3H, m), 4.32 (1H, d), 4.00 (2H, m), 3.76 (1H, d), 3.73 (3H, s), 1.94(1H, m), 1.73 (1H, m), 1.02 (2H, m).

Intermediate 84: Methyl(1aRS,7bSR)-5-[4-fluoro-2-(methoxycarbonylmethyl)benzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

A solution of methyl (2-chlorosulfonyl-5-fluorophenyl)acetate(Intermediate 85, 0.293 g) and methyl(1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate(Intermediate 42, 0.219 g) in pyridine (1 mL) and DCM (3 mL) was left tostand at room temperature for 4 days. The mixture was diluted with DCM,washed with 2M hydrochloric acid and filtered through a phase separator.The filtrate was concentrated in vacuo and the residue was purified bychromatography on silica, eluting with a mixture of ethyl acetate andcyclohexane with a gradient of 0-40% to give methyl(1aRS,7bSR)-5-[4-fluoro-2-(methoxycarbonylmethyl)-benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.438 g) as a colourless gum.

¹H NMR (CDCl₃) δ: 8.77 (1H, br, s), 7.84 (1H, dd), 7.22 (1H, d), 7.01(3H, m), 4.33 (1H, d), 4.01 (2H, s), 3.79 (1H, d), 3.76 (3H, s), 3.69(3H, s), 1.93 (1H, m), 1.73 (1H, m), 1.03 (2H, m).

Intermediate 85: Methyl (2-Chlorosulfonyl-5-fluorophenyl)acetate

Methyl (3-fluorophenyl)acetate (1.51 g) was added dropwise tochlorosulphonic acid (7 mL) with stirring and ice cooling. The coolingbath was removed and the mixture was allowed to stand at roomtemperature for 16 hours before being carefully added to a mixture ofice and ethyl acetate. The organic layer was separated, washed withwater, dried (MgSO₄) and filtered. The filtrate was concentrated invacuo and the residue was purified by chromatography on silica, elutingwith a mixture of ethyl acetate and cyclohexane with a gradient of 0-20%to give methyl (2-chlorosulfonyl-5-fluorophenyl)acetate (1.42 g) as awhite solid.

¹H NMR (CDCl₃) δ: 8.16 (1H, dd), 7.21 (2H, m), 4.19 (2H, s), 3.76 (3H,s).

Intermediate 86: Methyl(1aRS,7bSR)-5-[2-(1-ethylazetidin-3-yl)-4-fluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

A mixture of methyl(1aRS,7bSR)-5-[2-(azetidin-3-yl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 87, 0.216 g), iodoethane (0.078 g) and potassium carbonate(0.138 g) in acetonitrile (5 mL) was stirred at room temperature for 18hours. The mixture was evaporated to dryness and the residue waspurified by chromatography on silica, eluting with a mixture of methanoland DCM with a gradient of 0-15% to give methyl(1aRS,7bSR)-5-[2-(1-ethylazetidin-3-yl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(0.051 g).

¹H NMR (CDCl₃) δ: 7.97 (1H, dd), 7.62 (1H, dd), 7.24 (1H, d), 6.99 (1H,dt), 6.96 (1H, d), 4.35 (1H, d), 4.31 (1H, m), 3.79 (3H, s), 3.77 (1H,d), 3.58 (2H, m), 3.22 (2H, br, m), 2.53 (2H, q), 1.93 (1H, m), 1.74(1H, q), 0.99 (5H, m).

Intermediate 87: Methyl(1aRS,7bSR)-5-[2-(azetidin-3-yl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

A mixture of methyl(1aRS,7bSR)-5-{4-fluoro-2-[1-(2,2,2-trifluoroacetyl)azetidin-3-yl]benzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 88, 0.294 g) and potassium carbonate (0.155 g) in methanol(5 mL) and water (0.5 mL) was stirred at room temperature for 45minutes. The mixture was concentrated in vacuo and the residue wastriturated with 10% methanol in DCM and filtered. The filtrate wasconcentrated in vacuo and the residue was purified by chromatography onsilica, eluting with a mixture of methanol and DCM with a gradient of0-40% to give methyl(1aRS,7bSR)-5-[2-(azetidin-3-yl)-4-fluoro-benzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.216 g) as a pale yellow foam.

¹H NMR (CDCl₃) δ: δ: 7.94 (1H, dd), 7.54 (1H, dd), 7.27 (1H, d), 7.09(1H, dt), 6.99 (1H, d), 4.87 (1H, m), 4.32 (3H, m), 4.12 (2H, t), 3.78(1H, m), 3.73 (3H, s), 1.94 (1H, m), 1.73 (1H, m), 0.99 (2H, m).

Intermediate 88: Methyl(1aRS,7bSR)-5-{4-fluoro-2-[1-(2,2,2-trifluoroacetyl)azetidin-3-yl]benzenesulfonylamino})-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

A solution of methyl4-fluoro-2-[1-(2,2,2-trifluoroacetyl)azetidin-3-yl]benzenesulfonylchloride (Intermediate 89, 0.192 g) and methyl(1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(Intermediate 42, 0.122 g) in pyridine (1 mL) and DCM (3 mL) was left tostand at room temperature for 18 hours. The mixture was diluted withDCM, washed with 1M hydrochloric acid and filtered through a phaseseparator. The filtrate was concentrated in vacuo and the residue waspurified by chromatography on silica, eluting with a mixture of ethylacetate and cyclohexane with a gradient of 0-30% to give methyl(1aRS,7bSR)-5-{4-fluoro-2-[1-(2,2,2-trifluoro-acetyl)azetidin-3-yl]benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(0.294 g) as a colourless gum.

¹H NMR (CDCl₃) δ: 8.99 (1H, br, s), 7.99 (1H, m), 7.81 (2H, m), 7.06(2H, m), 4.68 (2H, m), 4.41 (1H, m), 4.34 (1H, d), 4.19 (1H, m), 4.08(1H, m), 3.79 (1H, m), 3.72 (3H, s), 1.94 (1H, m), 1.75 (1H, m), 1.02(2H, m).

Intermediate 89:4-Fluoro-2-[1-(2,2,2-trifluoroacetyl)-azetidin-3-yl]benzenesulfonylchloride

Chlorosulphonic acid (5 mL) was added to2,2,2-trifluoro-1-[3-(3-fluorophenyl)azetidin-1-yl]ethanone(Intermediate 90, 1.15 g) with stirring and ice cooling. The mixture wasstirred for 1 hour then poured carefully onto a mixture of ice and ethylacetate. The organic layer was washed with water and concentrated invacuo. The residue was purified by chromatography on silica, elutingwith a mixture of ethyl acetate and cyclohexane with a gradient of 0-20%to give4-fluoro-2-[1-(2,2,2-trifluoroacetyl)azetidin-3-yl]benzenesulfonylchloride (0.910 g) as a white solid.

¹H NMR (CDCl₃) δ: 8.22 (1H, m), 7.51 (1H, dd), 7.26 (1H, m), 4.95 (2H,m), 4.70 (1H, t), 4.42 (1H, m), 4.31 (1H, m).

Intermediate 90:2,2,2-Trifluoro-1-[3-(3-fluorophenyl)azetidin-1-yl]ethanone

A solution of tert-butyl 3-(3-fluorophenyl)azetidine-1-carboxylate(Intermediate 92, 2.51 g) in trifluoroacetic acid (15 mL) and DCM (15mL) was left to stand at room temperature for 30 minutes. The mixturewas concentrated in vacuo and the residue was azeotroped with toluene.The residue was dissolved in DCM (15 mL) and pyridine (5 mL) andtrifluoroacetic anhydride (3.15 g) was added. The mixture was left tostand at room temperature for 30 minutes, then washed with 1Mhydrochloric acid and filtered through a phase separator. The filtratewas concentrated in vacuo and the residue was purified by chromatographyon silica, eluting with a mixture of ethyl acetate and cyclohexane witha gradient of 0-20% to give2,2,2-trifluoro-1-[3-(3-fluorophenyl)azetidin-1-yl]ethanone (2.31 g) asa light brown oil.

¹H NMR (CDCl₃) δ: 7.36 (1H, m), 7.10 (1H, d), 7.02 (2H, m), 4.81 (1H,t), 4.57 (1H, t), 4.44 (1H, dd), 4.20 (1H, dd), 3.96 (1H, m).

Intermediate 91: tert-Butyl 3-(3-fluorophenyl)azetidine-1-carboxylate

A solution of 1,2-dibromoethane (0.30 g) in anhydrous DMF (25 ml) wasstirred with zinc dust (1.39 g) at 70° C. for 10 minutes then cooled toroom temperature and chlorotrimethylsilane was (0.155 g) added. Theresultant mixture was stirred at room temperature for 45 minutes.tert-Butyl 3-iodoazetidine-1-carboxylate (5 g) added and stirring wascontinued at 40° C. for 45 minutes then a solution of3-fluoroiodobenzene (4.08 g), tris(dibenzylideneacetone)dipalladium(0)(0.325 g) and tris(2-furyl)phosphine (0.165 g) in DMF (15 mL) was addedand the mixture was stirred at 70° C. for 3 hours. After cooling, themixture was diluted with water and ethyl acetate and filtered throughcelite. The organic layer was washed twice with water, dried (Na₂SO₄)and filtered. The filtrate was concentrated in vacuo and the residue waspurified by chromatography on silica, eluting with a mixture of ethylacetate and cyclohexane with a gradient of 0-10%. The crude product wasfurther purified by chromatography on silica, eluting with a mixture ofDCM and cyclohexane with a gradient of 0-100% to give tert-butyl3-(3-fluorophenyl)azetidine-1-carboxylate (2.52 g) as a colourless oil.

¹H NMR (CDCl₃) δ: 7.32 (1H, m), 6.90-7.11 (3H, m), 4.34 (2H, t), 3.95(2H, dd), 3.72 (1H, m), 1.48 (9H, s).

Intermediate 92: Methyl(1aRS,7bSR)-5-{2-[((R)-1-ethylpyrrolidin-3-ylcarbamoyl)methyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 80, startingfrom methyl(1aRS,7bSR)-5-(2-carboxymethyl-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate(Intermediate 83) and (R)-1-ethylpyrrolidin-3-ylamine ditrifluoroaceticacid salt (Intermediate 93) as a light brown foam.

LCMS (Method E) r/t 2.57 (M+H) 532.

Intermediate 93: (R)-1-Ethylpyrrolidin-3-ylamine ditrifluoroacetic acidsalt

Prepared by proceeding in a similar manner to Intermediate 81, startingfrom tert-butyl ((R)-1-ethylpyrrolidin-3-yl)carbamate as a light browngum which was used without further characterisation.

Intermediate 94: tert-Butyl ((R)-1-ethylpyrrolidin-3-yl)carbamate

Prepared by proceeding in a similar manner to Intermediate 82, startingfrom tert butyl (R)-pyrrolidin-3-yl-carbamate and iodoethane as a lightcoloured gum.

¹H NMR (CDCl₃) δ: 5.09 (2H, br, s), 4.25 (1H, br, s), 3.08 (1H, br, s),2.82 (2H, br, m), 2.69 (2H, br, q), 2.52 (1H, br, q), 2.35 (1H, m), 1.44(9H, s), 1.21 (3H, t).

Intermediate 95: Methyl(1aS,7bR)-5-[2-((R)-1-ethylpyrrolidin-3-ylmethyl)-4-fluoro-benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

A solution of methyl(1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 42, 0.257 g) in DCM (10 mL) and pyridine (5 mL) wastreated with a solution of2-((R)-1-ethylpyrrolidin-3-ylmethyl)-4-fluorobenzenesulfonyl chloride(Intermediate 96, 0.36 g) in DCM (10 mL) and the mixture was stirred atroom temperature overnight. The resultant mixture was evaporated todryness and the residue was re-dissolved in DCM, washed with water,dried (MgSO₄) and filtered. The filtrate was evaporated to dryness andthe residue was purified by chromatography on silica, eluting with amixture of methanol and DCM with a gradient of 0-10%, then flushed with100% methanol to give methyl(1aS,7bR)-5-[2-((R)-1-ethylpyrrolidin-3-ylmethyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.13 g) as a gum.

¹H NMR (CDCl₃) □: 7.88 (1H, br t), 7.23 (1H, d), 7.13 (1H, br d), 6.98(2H, m), 4.33 (1H, d), 3.79 (1H, d), 3.77 (3H, s), 3.20-2.90 (6H, m)2.24 (1H, br s), 2.04-1.18 (3H, br s), 1.93 (2H, dt), 1.74 (1H, q), 1.45(3H, t), 1.02 (2H, m).

Intermediate 96:2-((R)-1-Ethylpyrrolidin-3-ylmethyl)-4-fluorobenzenesulfonyl chloride

A solution of (R)-1-ethyl-3-(3-fluorobenzyl)pyrrolidine (Intermediate97, 0.24 g) in DCE (1.2 mL) was added carefully to chlorosulfonic acidand the mixture was stirred at room temperature for 2 hours. The mixturewas carefully poured into iced water and extracted with DCM, dried(MgSO₄) and filtered. The filtrate was evaporated to dryness to give2-((R)-1-ethyl-pyrrolidin-3-ylmethyl)-4-fluorobenzenesulfonyl chloride(0.36 g) as an oil which was used without further characterization.

Intermediate 97: (R)-1-Ethyl-3-(3-fluorobenzyl)-pyrrolidine

Ethyl bromide (0.22 g) was added to a suspension of3-(R)-(3-fluorobenzyl)pyrrolidine (Intermediate 98, 0.36 g) andpotassium carbonate (0.55 g) in acetonitrile and the mixture was stirredat room temperature for 2.5 hours. The mixture was diluted with ethylacetate, filtered and the filtrate was evaporated to dryness. Theresidue was triturated with DCM, the solvent was decanted off andevaporated to dryness to give (R)-1-ethyl-3-(3-fluorobenzyl)pyrrolidine(0.24 g) as an oil.

¹H NMR (CDCl₃) □δ: 7.22 (1H, m), 6.95 (1H, d), 6.88 (2H, m), 2.73-2.60(4H, m), 2.52-2.38 (4H, m), 2.17 (1H, dd), 1.97 (1H, m), 1.49 (1H, m),1.09 (3H, t).

Intermediate 98: 3-(R)-(3-Fluorobenzyl)pyrrolidine

Trifluoroacetic acid (10 mL) was added to a solution of tert butyl(R)-3-(3-fluorobenzyl)-pyrrolidine-1-carboxylate (Intermediate 99, 0.515g) in DCM (10 mL) and the mixture was stirred for 1 hour at roomtemperature. The mixture was evaporated to dryness and the residue waspartitioned between DCM and saturated aqueous NaHCO₃. The organicextract was separated, dried (MgSO₄) and filtered. The filtrate wasevaporated to dryness to give 3-(R)-(3-fluoro-benzyl)pyrrolidine (0.402g) as an oil.

¹H NMR (CDCl₃) □δ: 7.30-7.23 (2H, m), 6.94 (1H, d), 6.88 (1H, dt),3.45-3.16 (3H, br m), 2.90 (1H, m), 2.76 (2H, d), 2.63 (1H, m), 2.12(1H, m), 1.74 (1H, m).

Intermediate 99: tert-Butyl(R)-3-(3-fluorobenzyl)pyrrolidine-1-carboxylate

Nickel Iodide (0.147 g), trans-2-aminocyclohexanol HCl salt (0.74 g),3-fluorobenzene boronic acid (0.78 g) and sodium hexamethyldisilazide(0.208 g) were placed in a sealed tube and degassed and purged withargon. Isopropanol (8 mL) was added and the mixture was stirred at 40°C. for 5 minutes. A solution of tert-butyl(R)-3-iodomethylpyrrolidine-1-carboxylate (Intermediate 100, 1.44 g) inisopropanol (8 mL) was added and the mixture was stirred and heated at70° C. overnight. After cooling, the mixture was diluted with ethylacetate, filtered through Celite and the filtrate was evaporated todryness. The residue was purified by chromatography on silica, elutingwith a mixture of ethyl acetate and cyclohexane with a gradient of 0-60%to give tert-butyl (R)-3-(3-fluorobenzyl)pyrrolidine-1-carboxylate(0.515 g) as an oil.

¹H NMR (CDCl₃) □δ: 7.27-7.21 (2H, m), 6.95-6.84 (2H, m), 3.46 (2H, m),3.26 (1H, m), 2.98 (1H, dd), 2.67 (2H, m), 2.40 (1H, m), 1.92 (1H, m),1.58 (1H, m), 1.46 (9H, s).

Intermediate 100: tert-Butyl (R)-3-iodomethylpyrrolidine-1-carboxylate

Iodine (1.91 g) was added in portions to a vigorously stirred, icecooled suspension of imidazole (0.681 g) and triphenylphosphine (1.97 g)in diethyl ether (12 mL). The mixture was then stirred for 10 minutesbefore a solution of tert butyl(R)-3-hydroxymethylpyrrolidine-1-carboxylate (1 g) in dioxane (6 mL) wasadded dropwise. The resulting mixture was stirred at room temperatureovernight, then diluted with diethyl ether and filtered. The solid waswashed with diethyl ether and the combined filtrate was evaporated todryness. The residue was purified by chromatography on silica, elutingwith a mixture of ethyl acetate and pentane with a gradient of 0-20% togive tert-butyl (R)-3-iodomethylpyrrolidine-1-carboxylate (1.44 g) as anoil.

¹H NMR (CDCl₃) □δ: 3.64-3.46 (2H, m), 3.33 (1H, m), 3.19 (2H, d), 3.02(1H, dd), 2.49 (1H, m), 2.07 (1H, m), 1.65 (1H, m), 1.46 (9H, s).

Intermediate 101: Methyl(1aRS,7bSR)-5-{2-[((S)-1-ethylpyrrolidin-2-yl)cabonyl-aminomethyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

A mixture of methyl(1aRS,7bSR)-5-(2-aminomethyl-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 102, 0.515 g), HATU (0.483 g),(S)—N-ethylpyrrolidine-2-carboxylic acid (Intermediate 106, 0.182 g) andN,N-di-isopropyl-N-ethylamine (0.328 g) in dry DMF (25 mL) was stirredat room temperature for 2 hours. The mixture was concentrated undervacuum and the residue was diluted with water and extracted with ethylacetate, washed with water, dried (MgSO₄) and filtered. The filtrate wasevaporated to dryness and the residue was purified by chromatography onsilica, eluting with a mixture of methanol and DCM, with a graident of1-2% to give methyl(1aRS,7bSR)-5-{2-[((S)-1-ethylpyrrolidin-2-yl)cabonyl-aminomethyl]-4-fluorobenzenesulfonylamino})-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(0.505 g) as a glassy solid.

¹H NMR (CDCl₃) δ: 9.2-8.9 (1H, br s), 7.82 (2H, m), 7.24 (2H, m), 7.00(1H, dt), 6.95 (1H, dd), 4.75 (2H, m), 4.33 (1H, d), 3.99 (1H, br s),3.79 (1H, m), 3.77 (3H, s), 3.67 (1H, m), 3.15-2.87 (3H, m), 2.48 (1H,m), 2.02 (2H, m), 1.93 (2H, m), 1.74 (1H, m), 1.20 (3H, m), 1.02 (2H,m).

Intermediate 102: Methyl(1aRS,7bSR)-5-(2-aminomethyl)-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

A solution of potassium carbonate (2.1 g) in water was added to asolution of methyl(1aRS,7bSR)-5-(4-fluoro-2-trifluoroacetylaminomethyl)benzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 103, 1.53 g) in methanol (50 mL) and the resultant mixturewas stirred and heated at 45° C. for 4 hours. After cooling, the mixturewas concentrated under vacuum and the residue was diluted with water andsaturated with salt. The resultant solid was collected by filtration,washed with water and ethyl acetate then dried under vacuum at 50° C. togive methyl(1aRS,7bSR)-5-(2-aminomethyl)-4-fluoro-benzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(1.06 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 8.52 (1H, br s), 7.99 (1H, dd), 7.32 (2H, m), 6.89(1H, d), 6.74 (1H, d), 4.32 (2H, s), 4.17 (1H, d), 3.70 (3H, s), 3.64(1H, d), 1.82 (1H, m), 1.65 (1H, m), 0.89 (1H, m), 0.61 (1H, m).

Intermediate 103: Methyl(1aRS,7bSR)-5-(4-fluoro-2-trifluoroacetylaminomethyl)benzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Methyl (1aRS,7bSR)-5amino-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 42, 0.972 g) was added to a solution of4-fluoro-2-(trifluoroacetylaminomethyl)-benzenesulfonyl chloride(Intermediate 104, 1.53 g) in DCM (25 mL) and pyridine (6 mL). Theresultant mixture was stirred at room temperature for 2 hours. Themixture was diluted with DCM, washed with water, HCl (1M), water, dried(MgSO₄) and filtered. The filtrate was evaporated to dryness and theresidue was purified by chromatography on silica, eluting with a mixtureof ethyl acetate and pentane with a gradient of 5-30% to give methyl(1aRS,7bSR)-5-(2-trifluoroacetylaminomethyl)-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(1.76 g) as a glassy foam.

¹H NMR (CDCl₃) δ: 9.04 (1H, br s), 7.83 (1H, dd), 7.49 (1H, br t), 7.30(1H, dd), 7.29 (1H, d), 7.09 (1H, d), 7.06 (1H, dt), 4.61 (2H, d), 4.34(1H, d), 3.78 (1H, dd), 3.73 (3H, s), 1.95 (1H, m), 1.75 (1H, m), 1.04(2H, m).

Intermediate 104: 4-Fluoro-2-(trifluoroacetylaminomethyl)benzenesulfonylchloride

3-Fluoro-N-trifluoroacetylbenzylamine (Intermediate 105, 1.1 g) wasadded portionwise to chlorosulfonic acid (5 mL), while stirring andcooling in an ice bath. On completion of the addition, the ice bath wasremoved and the mixture was allowed to come to room temperature thenheated to 70° C. for 3 hours. After cooling, the mixture was slowlyadded to ice and the resultant suspension was extracted with ethylacetate, washed with water, dried (MgSO₄) and filtered. The filtrate wasevaporated to dryness to give4-fluoro-2-(trifluoroacetylaminomethyl)benzenesulfonyl chloride (1.53 g)as a brown solid.

¹H NMR (CDCl₃) δ: 8.18 (1H, dd), 7.47 (1H, m), 7.29 (1H, m), 7.18 (1H,br s), 4.92 (2H, d).

Intermediate 105: 3-Fluoro-N-trifluoroacetylbenzylamine

Trifluoroacetic anhydride (5.05 g) was added dropwise to an ice-cooledsolution of 3-fluorobenzylamine (2.5 g) and triethylamine (2.22 g) inethyl acetate (75 mL) while maintaining the temperature below 10° C. Themixture was stirred at 0-5° C. for 1 hour then allowed to warm to roomtemperature and stirred for 2 hours. Water was added and the layers wereseparated. The organic layer was washed with water, dried (MgSO₄) andfiltered. The filtrate was evaporated to dryness to give3-fluoro-N-trifluoroacetylbenzylamine (4.58 g) as an oil whichcrystallised on standing to a white solid.

¹H NMR (CDCl₃) δ: 7.34 (1H, m), 7.03 (3H, m), 6.72 (1H, br s), 4.53 (2H,d).

Intermediate 106: (S)—N-Ethylpyrrolidine-2-carboxylic acid

Palladium on carbon (10%, 0.2 g) was added to a solution of benzyl(S)—N-ethylpyrrolidine-2-carboxylate (Intermediate 107, 0.603 g) underan atmosphere of nitrogen. The mixture was then hydrogenated at 4Bar for3 hours. The mixture was filtered through Celite and the filtrate wasevaporated to dryness to give (S)—N-ethylpyrrolidine-2-carboxylic acid(0.378 g) as a straw coloured gummy solid.

¹H NMR (CDCl₃) δ: 4.01 (1H, m), 3.78 (1H, m), 3.31 (1H, m), 3.18 (1H,m), 2.87 (1H, m), 2.38 (1H, m), 2.27 (1H, m), 2.02 (2H m), 1.39 (3H, t).

Intermediate 107: Benzyl (S)—N-ethylpyrrolidine-2-carboxylatehydrochloride

Iodoethane (1.34 g) was added to a mixture of benzyl(S)-pyrrolidine-2-carboxylate (1.0 g) and potassium carbonate (1.77 g)in dry DMF (7 mL) and the resultant mixture was stirred at roomtemperature for 3 days. The mixture was diluted with water, extractedwith ethyl acetate, washed with water, dried (MgSO₄) and filtered. Thefiltrate was evaporated to dryness and the residue was purified bychromatography on silica, eluting with a mixture of ethyl acetate andpentane with a gradient of 10-20% to give benzyl(S)—N-ethylpyrrolidine-2-carboxylate (0.643 g) as a pale straw colouredoil.

¹H NMR (CDCl₃) δ: 7.35 (5H, m), 5.17 (2H, s), 3.19 (2H, m), 2.74 (1H,m), 2.45 (1H, m), 2.34 (1H, m), 2.12 (1H, m) 1.93 (2H, m), 1.81 (1H, m),1.10 (3H, t).

Intermediate 108: Methyl(1aRS,7bSR)-5-[2-(4-dimethylaminobutyrylamino)-4-fluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

A mixture of methyl(1aRS,7bSR)-5-{N-[methoxycarbonyl]-N-[2-(4-chlorobutyryl-amino)-4-fluorobenzenesulfonyl]amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(Intermediate 109, 0.15 g) and dimethylamine (30% aqueous solution, 5mL) in acetonitrile (10 mL) was stirred and heated at 40° C. for 10hours. After cooling, the mixture was concentrated under vacuum and theresidue was extracted with a mixture of ethyl acetate and THF (50%),dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness andthe residue was purified by thick layer chromatography on silica,eluting with a mixture of methanol and DCM (10%) to give methyl(1aRS,7bSR)-5-[2-(4-dimethylaminobutyrylamino)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(0.14 g) as a yellow oil.

LCMS (Method D) r/t 1.24 (M+H) 506.

Intermediate 109: Methyl(1aRS,7bSR)-5-{N-[methoxycarbonyl]-N-[2-(4-chlorobutyryl-amino)-4-fluorobenzenesulfonyl]amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

4-Chlorobutyryl chloride (3.0 g) was added to a stirred, cooled solutionof methyl(1aRS,7bSR)-5-[N-(methoxycarbonyl)-N-(2-amino-4-fluorobenzenesulfonyl]amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(Intermediate 110, 0.135 g) and triethylamine (1.0 g) in THF (10 mL) at0° C. On completion of the addition, the mixture was stirred at roomtemperature for 4 hours. Saturated aqueous sodium bicarbonate was addedand the mixture was extracted with ethyl acetate, dried (Na₂SO₄) andfiltered. The filtrate was evaporated to dryness and the residue waspurified by chromatography on silica, eluting with a mixture of ethylacetate and petroleum ether, with a gradient of 20-25% to give methyl(1aRS,7bSR)-5-{N-[methoxycarbonyl]-N-[2-(4-chlorobutyrylamino)-4-fluoro-benzenesulfonyl]amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(0.15 g) as a yellow oil.

LCMS (Method D) r/t 1.72 (M+H) 555.

Intermediate 110: Methyl(1aRS,7bSR)-5-[N-(methoxycarbonyl)-N-(2-amino-4-fluorobenzene-sulfonyl)amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

A mixture of methyl(1aRS,7bSR)-5-[N-(methoxycarbonyl)-N-(4-fluoro-2-nitrobenzene-sulfonyl)amino]-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate(Intermediate 111, 0.2 g), zinc (0.54 g) and acetic acid (0.5 g) inethanol (20 mL) was stirred and heated at reflux for 1 hour. Aftercooling, the solid was filtered off and the filtrate was evaporated todryness. The residue was treated with saturated aqueous sodiumbicarbonate and extracted with ethyl acetate, dried (Na₂SO₄) andfiltered. The filtrate was evaporated to dryness and the residue waspurified by chromatography on silica, eluting with a mixture of ethylacetate and petroleum ether with a gradient of 30-50% to give methyl(1aRS,7bSR)-5-[N-(methoxycarbonyl)-N-(2-amino-4-fluorobenzenesulfonyl)amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.15 g) as a white solid.

¹H NMR (CDCl₃) δ: 7.74 (1H, m), 7.36 (1H, d), 6.95 (1H, d), 6.47 (1H,m), 6.39 (1H, d), 5.37 (2H, m), 4.42 (1H, m), 3.91 (1H, d), 3.74 (3H,2s), 3.70 (3H, 2s), 2.06 (1H, m), 1.84 (1H, m), 1.28 (1H, m), 1.15 (1H,m).

Intermediate 111: Methyl(1aRS,7bSR)-5-[N-(methoxycarbonyl)-N-(4-fluoro-2-nitrobenzene-sulfonyl)amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

A solution of methyl(1aRS,7bSR)-5-(4-fluoro-2-nitrobenzenesulfonylamino)-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate(Intermediate 112, 0.25 g) in THF (10 mL) was added dropwise withstirring to a cooled suspension of sodium hydride (0.1 g) in THF (5 mL)at 0° C. On completion of the addition, the mixture was stirred at roomtemperature for 30 minutes. Methyl chloroformate (0.3 g) was addeddropwise and the mixture was stirred at room temperature for 1.5 hours.Saturated aqueous sodium bicarbonate was added and the mixture wasextracted with ethyl acetate, dried (Na₂SO₄) and filtered. The filtratewas evaporated to dryness and the residue was purified by chromatographyon silica, eluting with a mixture of ethyl acetate and petroleum etherto give methyl(1aRS,7bSR)-5-[N-(methoxycarbonyl)-N-(4-fluoro-2-nitrobenzenesulfonyl)amino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(0.2 g) as a white solid.

LCMS (Method D) r/t 1.58 (M+H) 481.

Intermediate 112: Methyl(1aRS,7bSR)-5-(4-fluoro-2-nitrobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

A mixture of methyl(1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(Intermediate 42, 0.1 g), 4-fluoro-2-nitrobenzenesulfonyl chloride(0.115 g) and pyridine (2 mL) in DCM (5 mL) was stirred at roomtemperature overnight. The mixture was concentrated under vacuum and theresidue was partitioned between ethyl acetate and water. The organiclayer was dried (Na₂SO₄) and filtered and the filtrate was evaporated todryness. The residue was purified by chromatography on silica, elutingwith a mixture of ethyl acetate and petroleum ether (20%) to give methyl(1aRS,7bSR)-5-(4-fluoro-2-nitrobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.11 g) as a yellow oil.

¹H NMR (CDCl₃) δ: 8.56 (1H, br s), 7.92 (1H, m), 7.55 (1H, dd), 7.31(2H, m), 7.24 (1H, m), 4.34 (1H, d), 3.85 (3H, s), 3.82 (1H, d), 1.98(1H, m), 1.74 (1H, m), 1.08 (2H, m).

Intermediate 113: Methyl(1aS,7bR)-5-[2-((S)-1-ethyl-pyrrolidin-3-ylmethyl)-4-fluoro-benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

A solution of methyl5-amino-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 42, 0.19 g) in DCM (10 mL) and pyridine (3.5 mL) wastreated with a solution of2-((S)-1-ethylpyrrolidin-3-ylmethyl)-4-fluorobenzenesulfonyl chloride(Intermediate 114, 0.26 g) in DCM (5 mL) and the mixture was stirred andheated at 40° C. for 1 hour. The resultant mixture was evaporated todryness and the residue was purified by chromatography on silica,eluting with a mixture of DCM and methanol with a gradient of 0-25%,then flushed with 100% methanol to give methyl(1aS,7bR)-5-[2-((S)-1-ethylpyrrolidin-3-ylmethyl)-4-fluoro-benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.107 g) as a gum.

LCMS (Method A) r/t 2.29 (M+H) 489.

Intermediate 114:2-((S)-1-Ethylpyrrolidin-3-ylmethyl)-4-fluorobenzenesulfonyl chloride

Prepared by proceeding in a similar manner to Intermediate 96, startingfrom (S)-1-ethyl-3-(3-fluorobenzyl)pyrrolidine (Intermediate 115).

LCMS (Method A) r/t 1.95 (M+H) 308.

Intermediate 115: (S)-1-Ethyl-3-(3-fluorobenzyl)pyrrolidine

Prepared by proceeding in a similar manner to Intermediate 97 startingwith 3-(S)-(3-fluoro-benzyl)pyrrolidine (Intermediate 116).

¹H NMR (CDCl₃) □δ: 7.22 (1H, m), 6.95 (1H, d), 6.88 (2H, m), 2.81-2.62(4H, br m), 2.61-2.39 (4H, br m), 2.21 (1H, br s), 1.99 (1H, m), 1.52(1H, m), 1.11 (3H, t).

Intermediate 116: 3-(S)-(3-Fluorobenzyl)-pyrrolidine

Prepared by proceeding in a similar manner to Intermediate 98 startingwith tert-butyl (S)-3-(3-fluorobenzyl)-pyrrolidine-1-carboxylate(intermediate 117).

¹H NMR (CDCl₃) δ: 7.27 (1H, m), 6.96-6.84 (3H, m), 3.32 (1H, m), 3.25(1H, dd), 3.16 (1H, m), 2.83 (1H, m), 2.73 (2H, d), 2.58 (1H, m), 2.08(1H, m), 1.68 (1H, m).

Intermediate 117: tert-Butyl(S)-3-(3-fluorobenzyl)-pyrrolidine-1-carboxylate

Prepared by proceeding in a similar manner to Intermediate 99 startingwith tert-butyl (S)-3-iodomethylpyrrolidine-1-carboxylate (Intermediate118).

¹H NMR (CDCl₃) 58 δ: 7.27 (1H, m), 6.97-6.83 (3H, m), 3.46 (2H, m), 3.25(1H, m), 2.98 (1H, m), 2.67 (2H, m), 2.40 (1H, m), 1.91 (1H, m), 1.58(1H, m), 1.45 (9H, s).

Intermediate 118: tert-Butyl (S)-3-iodomethylpyrrolidine-1-carboxylate

Prepared by proceeding in a similar manner to Intermediate 100 startingwith tert-butyl (S)-3-hydroxymethylpyrrolidine-1-carboxylate.

¹H NMR (CDCl₃) □δ: 3.59 (1H, dd), 3.51 (1H, m), 3.33 (1H, m), 3.19 (2H,d), 3.02 (1H, dd), 2.49 (1H, m), 2.07 (1H, m), 1.65 (1H, m), 1.46 (9H,s).

Intermediate 119: tert-Butyl(1aRS,7bSR)-5-{2-[N-(2,4-dimethoxybenzyl)-N-(3-dimethyl-aminopropyl)carbamoyl]benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

A solution of N-(2,4-dimethoxybenzyl)-N-(3-dimethylaminopropyl)amine(Intermediate 120, 0.179 g) in DCM (2 mL) was added dropwise withstirring to a cooled solution of 2-chlorosulfonylbenzoyl chloride(Intermediate 121, 0.17 g) in DCM (20 mL) at 0° C. The mixture wasstirred at 0° C. for 1 hour then a solution of tert-butyl(1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydro-cyclopropa-[c]chromene-4-carboxylate(Intermediate 122, 0.185 g) in DCM (2 mL) was added. The resultantmixture was stirred and heated at 30-35° C. overnight. After cooling,the mixture was concentrated under vacuum and the residue was purifiedby HPLC (C18) to give tert-butyl(1aRS,7bSR)-5-{2-[N-(2,4-dimethoxybenzyl)-N-(3-dimethylaminopropyl)carbamoyl]-benzenesulfonylamino}-1,1a,2,7b-tetrahydro-cyclopropa-[c]chromene-4-carboxylate(0.03 g) as a yellow oil.

LCMS (Method D) r/t 3.16 (M+H) 680.

Intermediate 120: N-(2,4-Dimethoxybenzyl)-N-(3-dimethylaminopropyl)amine

A mixture of 3-dimethylaminopropylamine (3.06 g),2,4-dimethoxybenzaldehyde (6.0 g) and sodium triacetoxyborohydride (9.54g) in methanol (20 mL) was stirred at room temperature for 10 hours. Themixture was concentrated under vacuum and the residue was dissolved inethyl acetate and washed with water and brine, dried (Na₂SO₄) andfiltered. The filtrate was evaporated to dryness to giveN-(2,4-dimethoxybenzyl)-N-(3-dimethylaminopropyl)amine (7.2 g) as abrown oil which was used directly without further characterisation.

Intermediate 121: 2-Chlorosulfonylbenzoyl chloride

A mixture of 1,1-dioxo-1H-llambda*6*benzo[c][1,2]oxathiol-3-one (4.5 g)and phosphorous pentachloride (15 g) was stirred and heated at 60° C.overnight. After cooling, a mixture of ice and water was added and thesolution was extracted with DCM, dried (Na₂SO₄) and filtered. Thefiltrate was evaporated to dryness to give 2-chlorosulfonylbenzoylchloride (5 g) as a yellow solid which was used without furthercharacterisation.

Intermediate 122: tert-Butyl(1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

Sodium borohydride (0.32 g) was added in portions to a stirred solutionof tert-butyl(1aRS,7bSR)-5-(trifluoroacetylamino)-1,1a,2,7b-tetrahydro-cyclopropa-[c]chromene-4-carboxylate(Intermediate 123, 0.5 g) in ethanol (20 mL). The resultant mixture wasstirred at room temperature for 1 hour then concentrated under vacuum.The residue was purified by chromatography on silica, eluting with amixture of ethyl acetate and petroleum ether with a gradient of 2-4% togive tert-butyl(1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(0.2 g) as a white solid.

¹H NMR (CDCl₃) δ: 7.04 (1H, d), 6.25 (1H, d), 4.57 (2H, br s), 4.32 (1H,d), 3.87 (1H, d), 1.86 (1H, m), 1.65 (1H, m), 1.60 (9H, s), 0.95 (2H,m).

Intermediate 123: tert-Butyl(1aRS,7bSR)-5-(trifluoroacetylamino)-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate

A mixture of(1aRS,7bSR)-5-(trifluoroacetylamino)-1,a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid (Intermediate 124, 0.97 g), DMAP (0.2 g), dicyclohexyl carbodiimide(1.33 g) and di-tert-butyl dicarbonate (3.51 g) in tert-butanol (20 mL)was stirred and heated at reflux for 7 hours. After cooling, the mixturewas concentrated under vacuum and the residue was purified bychromatography on silica, eluting with a mixture of ethyl acetate andpetroleum ether (2%) to give tert-butyl(1aRS,7bSR)-5-(trifluoroacetylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.5 g) as a yellow oil.

¹H NMR (CDCl₃) δ: 10.47 (1H, br s), 7.89 (1H, d), 7.34 (1H, d), 4.39(1H, d), 3.88 (1H, d), 2.02 (1H, m), 1.77 (1H, m), 1.60 (9H, s), 1.09(2H, m).

Intermediate 124:(1aRS,7bSR)-5-(Trifluoroacetylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid

Trifluoroacetic anhydride (2.98 g) was added dropwise to a stirred,cooled solution of(1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydro-cyclopropa-[c]chromene-4-carboxylicacid (Intermediate 125, 0.97 g) and triethylamine (2.39 g) in THF (20mL). The resultant mixture was stirred at room temperature for 30minutes. Water was added and the mixture was extracted with ethylacetate, dried (Na₂SO₄) and filtered. The filtrate was evaporated todryness and the residue was purified by chromatography on silica,eluting with a mixture of ethyl acetate and petroleum ether (2%) to give(1aRS,7bSR)-5-(trifluoroacetylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylicacid (0.97 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.92 (1H, d), 7.28 (1H, d), 4.54 (1H, d), 3.94 (1H,d), 2.27 (1H, m), 2.02 (1H, m), 1.21 (1H, m), 0.95 (1H, m).

Intermediate 125:(1aRS,7bSR)-5-Amino-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylicacid

A mixture of methyl(1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 42, 1.0 g) and lithium hydroxide monohydrate (0.96 g) indioxane (16 mL) and water (14 mL) was stirred and heated at 90° C. for 1hour. After cooling, the mixture was concentrated under vacuum and theresidue was diluted with water and neutralised to pH7 with formic acid.The mixture was then extracted with ethyl acetate, dried (Na₂SO₄) andfiltered and the filtrate was evaporated to dryness to give(1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydro-cyclopropa-[c]chromene-4-carboxylicacid (0.97 g) as a yellow oil.

LCMS (Method D) r/t 2.13 (M+H) 206.

Intermediate 126: Methyl(1aRS,7bSR)-5-(2-{[N—((S)-1-ethylpyrrolidin-3-yl)-N-methylcarbamoyl]-methyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

EDAC (0.058 g) was added to a stirred solution of methyl(1aRS,7bSR)-5-(2-carboxymethyl-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 83, 0.109 g) in DCM (3 mL) and the mixture was stirred atroom temperature for 10 minutes. A solution ofN—((S)-1-ethylpyrrolidin-3-yl)-N-methylamine dihydrochloride(Intermediate 127, 0.102 g) and triethylamine (0.151 g) in DCM (3 mL)was added and the mixture stirred for 17 hours. The mixture wasevaporated in vacuo and the residue was dissolved in dioxane (4 mL) andthe mixture was heated at 75° C. for 20 hours. After cooling, themixture was diluted with DCM and water and filtered through a phaseseparator. The filtrate was evaporated in vacuo and the residue wascombined with an identical reaction carried out earlier. The materialwas purified by chromatography on silica, eluting with a mixture ofmethanol and DCM with a gradient of 0-50% to give methyl(1aRS,7bSR)-5-(2-{[((S)-1-ethylpyrrolidin-3-yl)methylcarbamoyl]methyl}-4-fluoro-benzenesulfonylamino)-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate(0.48 g) as a light brown foam.

LCMS (Method E) r/t 2.65 (M+H) 546.

Intermediate 127: N—((S)-1-Ethylpyrrolidin-3-yl)-N-methylaminedihydrochloride

A mixture of benzyl N—((S)-1-ethylpyrrolidin-3-yl)-N-methylcarbamate(Intermediate 128, 0.682 g) and 10% palladium on carbon (0.10 g) inethanol (20 mL) was stirred at room temperature under an atmosphere ofhydrogen for 3 hours. The mixture was filtered, and concentratedhydrochloric acid (2 mL) was added. The solution was evaporated in vacuothen redissolved in a mixture of toluene and ethanol then re-evaporatedto give N—((S)-1-ethylpyrrolidin-3-yl)-N-methylamine dihydrochloride(0.531 g) as a light coloured, viscous oil which was used withoutfurther characterisation.

Intermediate 128: BenzylN—((S)-1-ethylpyrrolidin-3-yl)-N-methylcarbamate

A mixture of benzyl N-methyl-(S)-pyrrolidin-3-ylcarbamate (Intermediate129, 1.28 g), iodoethane (0.853 g), and potassium carbonate (1.51 g) inacetonitrile (12 mL) was stirred at room temperature for 4 hours. Themixture was evaporated in vacuo and the residue was basified with 5Msodium hydroxide and filtered through a phase separator. The filtratewas concentrated in vacuo and the residue was purified by chromatographyon silica, eluting with a mixture of methanol and DCM with a gradient of0-30% to give benzyl N—((S)-1-ethylpyrrolidin-3-yl)-N-methylcarbamate(0.686 g) as a colourless oil.

¹H NMR (CDCl₃) δ: 7.35 (5H, m), 5.13 (2H, s), 4.84 (1H, br, s), 2.91(3H, s), 2.30-2.82 (6H, m), 2.12 (1H, br, m), 1.79 (1H, m), 1.10 (3H,t).

Intermediate 129: Benzyl N-methyl-(S)-pyrrolidin-3-ylcarbamate

A solution of tert-butyl(S)-3-(N-benzyloxycarbonyl-N-methylamino)pyrrolidine-1-carboxylate(Intermediate 130, 1.81 g) in trifluoroacetic acid (8 mL) and DCM (8 mL)was left to stand at room temperature for 30 minutes. The resultantmixture was concentrated in vacuo and the residue was dissolved in DCMand brine, basified with 2M sodium hydroxide and filtered through aphase separator. The filtrate was concentrated in vacuo to give benzylN-methyl-(S)-pyrrolidin-3-ylcarbamate (1.46 g) as a light coloured oil.

¹H NMR (CDCl₃) δ: 7.35 (5H, m), 5.14 (2H, s), 4.68 (1H, br, m), 3.08(2H, m), 2.88 (3H, s), 2.76-2.95 (3H, m), 2.01 (1H, m), 1.75 (1H, m).

Intermediate 130: tert-Butyl(S)-3-(N-benzyloxycarbonyl-N-methylamino)pyrrolidine-1-carboxylate

Sodium hydride (60% oil dispersion, 0.32 g) was added to a stirredsolution of tert-butyl(S)-3-benzyloxycarbonylaminopyrrolidine-1-carboxylate (preparedaccording to Cheng et al, WO2007 142585, 1.73 g) in THF (20 mL) and themixture was stirred for 15 minutes. Iodomethane (1.85 g) was added andthe mixture was stirred at room temperature for 1 hour. Methanol wascarefully added to destroy the excess sodium hydride then ethyl acetateand water were added and the organic layer was washed with brine, dried(Na₂SO₄), filtered. The filtrate was concentrated in vacuo to givetert-butyl(S)-3-(N-benzyloxycarbonyl-N-methylamino)pyrrolidine-1-carboxylate (1.66g) as a pale coloured oil.

¹H NMR (CDCl₃) δ: 7.36 (5H, m), 5.15 (2H, s), 4.79 (1H, br, s), 3.54(2H, br, m), 3.11-3.38 (2H, br, m), 2.86 (3H, s), 1.98 (2H, m), 1.46(9H, s).

Intermediate 131: Methyl(1aRS,7bSR)-5-(2-{[N—((R)-1-ethylpyrrolidin-3-yl)-N-methylcarbamoyl]methyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 126, startingfrom methyl(1aRS,7bSR)-5-(2-carboxymethyl-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate(Intermediate 83) and N—((R)-1-ethylpyrrolidin-3-yl)-N-methylaminedihydrochloride (Intermediate 132) as a light brown foam.

LCMS (Method E) r/t 2.63 (M+H) 546 Intermediate 132:N—((R)-1-Ethylpyrrolidin-3-yl)-N-methylamine dihydrochloride

Prepared by proceeding in a similar manner to Intermediate 127, startingfrom benzyl N—((R)-1-ethylpyrrolidin-3-yl)-N-methylcarbamate(Intermediate 133) as a light coloured viscous oil, which was usedwithout further characterization.

Intermediate 133: BenzylN—((R)-1-ethylpyrrolidin-3-yl)-N-methylcarbamate

Prepared by proceeding in a similar manner to Intermediate 128, startingfrom benzyl N-methyl-(R)-pyrrolidin-3-ylcarbamate (I including bridgedor fused rings, and intermediate 134) and iodoethane, as a lightcoloured oil.

¹H NMR (CDCl₃) δ: 7.35 (5H, m), 5.13 (2H, s), 4.84 (1H, br, s), 2.91(3H, s), 2.30-2.87 (6H, m), 2.12 (1H, br, m), 1.80 (1H, m), 1.10 (3H,t).

Intermediate 134: Benzyl N-methyl-(R)-pyrrolidin-3-ylcarbamate

Prepared by proceeding in a similar manner to Intermediate 129, startingfrom tert-butyl(R)-3-(N-benzyloxycarbonyl-N-methylamino)-pyrrolidine-1-carboxylate(Intermediate 135) as a plane coloured oil.

¹H NMR (CDCl₃) δ: 7.35 (5H, m), 5.14 (2H, s), 4.79 (1H, br, s), 3.08(2H, m), 2.88 (3H, s), 2.76-2.95 (3H, m), 2.01 (1H, m), 1.75 (1H, m).

Intermediate 135: tert-Butyl(R)-3-(N-benzyloxycarbonyl-N-methylamino)pyrrolidine-1-carboxylate

Prepared by proceeding in a similar manner to Intermediate 130, startingfrom tert-butyl (R)-3-benzyloxycarbonylaminopyrrolidine-1-carboxylate(prepared according to Zhou et al, US 2008 0293771) and iodomethane, asa pale coloured oil.

¹H NMR (CDCl₃) δ: 7.35 (5H, m), 5.15 (2H, s), 4.69 (1H, br, s), 3.54(2H, br, m), 3.11-3.38 (2H, br, m), 2.86 (3H, s), 1.98 (2H, m), 1.46(9H, s).

Intermediate 136: 2((S)-1-Ethylpyrrolidin-2-yl)ethylamine

((S)-1-Acetylpyrrolidin-2-yl)acetonitrile (Intermediate 137, 1.0 g) wasadded potionwise to a stirred, cooled solution of lithium aluminiumhydride (0.36 g) in THF (30 mL) under an atmosphere of nitrogen whilemaintaining the temperature at 0° C. The mixture was allowed to warm toroom temperature then heated at reflux for 2 hours. After cooling,ethanol (4 mL) was added dropwise and the resultant solid was filteredoff. The filtrate was evaporated to dryness to give2((S)-1-ethylpyrrolidin-2-yl)ethylamine (0.6 g) as a colourless oil.

¹H NMR (D₂O) δ: 3.59 (1H, m), 3.37 (2H, m), 3.01 (4H, m), 2.24 (2H, m),1.98 (3H, m), 1.65 (1H, m), 1.21 (3H, t).

Intermediate 137: ((S)-1-Acetylpyrrolidin-2-yl)acetonitrile

Acetyl chloride (8.6 g) was added dropwise to a stirred, cooled solutionof ((S)-pyrrolidin-2-yl)acetonitrile hydrochloride (Intermediate 138,8.0 g) and triethylamine (16.5 g) in DCM (80 mL) while maintaining thetemperature at 0° C. The resultant solution was stirred at 0° C. for 30minutes. Water was added and the layers were separated. The aqueouslayer was further extracted with DCM and the combined organic layerswere washed with brine, dried (Na₂SO₄) and filtered. The filtrate wasevaporated to dryness and the residue was purified by HPLC (C18) to give((S)-1-acetylpyrrolidin-2-yl)acetonitrile (5.0 g) as a light yellow oilwhich was used directly without further characterisation.

Intermediate 138: ((S)-Pyrrolidin-2-yl)acetonitrile hydrochloride

A solution of tert-butyl (S)-2-cyanomethylpyrrolidine-1-carboxylate(Intermediate 139, 13.0 g) in methanol (130 mL) and concentratedhydrochloric acid (13 mL) was stirred and heated at 40° C. overnight.After cooling, the mixture was concentrated under vacuum and the residuewas diluted with toluene and reconcentrated. Ethanol (20 mL) was addedand the resultant solid was collected by filtration and washed withhexane to give ((S)-pyrrolidin-2-yl)acetonitrile hydrochloride (8.0 g)as a white solid.

LCMS (Method D) r/t 0.50 (M+H) 111.

Intermediate 139: tert-Butyl (S)-2-cyanomethylpyrrolidine-1-carboxylate

Sodium cyanide (8.2 g) was added to a solution of tert-butyl(S)-2-(4-methylbenzenesulfonyloxymethyl)pyrrolidine-1-carboxylate(Intermediate 140, 29.6 g) in DMSO (300 mL) and the resultant mixturewas stirred and heated at 90° C. for 5.5 hours. After cooling, themixture was treated with saturated aqueous iron (II) sulphate solutionand the mixture was stirred for a further 5 hours then extracted withethyl acetate. The organic layer was washed with brine, dried (Na₂SO₄)and filtered. The filtrate was evaporated to dryness and the residue waspurified by chromatography on silica, eluting with a mixture of ethylacetate and petroleum ether (5%) to give tert-butyl(S)-2-cyanomethylpyrrolidine-1-carboxylate (13.0 g) as a light yellowoil which was used without further characterisation.

Intermediate 140: tert-Butyl(S)-2-(4-methylbenzenesulfonyloxymethyl)pyrrolidine-1-carboxylate

4-Methylbenzenesulfonyl chloride (22.7 g) was added portionwise to astirred, cooled solution of tert-butyl(S)-2-hydroxyoxymethylpyrrolidine-1-carboxylate (20.0 g) in pyridine (70mL) while maintaining the temperature at 0° C. The resultant mixture wasstirred at room temperature overnight. The mixture was concentratedunder vacuum and the residue was dissolved in DCM and washed withsaturated aqueous sodium bicarbonate solution and brine, dried (Na₂SO₄)and filtered. The filtrate was evaporated to dryness to give tert-butyl(S)-2-(4-methylbenzenesulfonyl-oxymethyl)pyrrolidine-1-carboxylate (34g) as a yellow oil which was used without further characterisation.

Intermediate 141: 2-((R)-1-Ethylpyrrolidin-2-yl)ethylamine

Prepared by proceeding in a similar manner to Intermediate 136, startingfrom ((S)-1-acetylpyrrolidin-2-yl)acetonitrile (Intermediate 142) andused without further characterisation.

Intermediate 142: ((R)-1-Acetylpyrrolidin-2-yl)acetonitrile

Prepared by proceeding in a similar manner to Intermediate 137, startingfrom ((R)-pyrrolidin-2-yl)acetonitrile hydrochloride (Intermediate 143)and used without further characterisation.

Intermediate 143: ((R)-Pyrrolidin-2-yl)acetonitrile hydrochloride

Prepared by proceeding in a similar manner to Intermediate 138, startingfrom tert-butyl (R)-2-cyanomethylpyrrolidine-1-carboxylate (Intermediate144) and used without further characterisation.

Intermediate 144: tert-Butyl (R)-2-cyanomethylpyrrolidine-1-carboxylate

Prepared by proceeding in a similar manner to Intermediate 139, startingfrom tert-butyl(R)-2-(4-methylbenzenesulfonyloxymethyl)pyrrolidine-1-carboxylate(Intermediate 145) and used without further characterisation.

Intermediate 145: tert-Butyl(R)-2-(4-methylbenzenesulfonyloxymethyl)pyrrolidine-1-carboxylate

Prepared by proceeding in a similar manner to Intermediate 140, startingfrom tert-butyl (R)-2-hydroxymethylpyrrolidine-1-carboxylate and usedwithout further characterisation.

Intermediate 146: Methyl(1aRS,7bSR)-5-(2-{[((R)-1-ethylpyrrolidine-2-yl)carbonylamino]-methyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 101, startingfrom methyl(1aRS,7bSR)-5-(2-aminomethyl-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate(Intermediate 102) and (R)-1-ethylpyrrolidine-2-carboxylic acid(Intermediate 147) as a solid.

LCMS (Method B) r/t 2.37 (M+H) 532 Intermediate 147:(R)-1-Ethyl-pyrrolidine-2-carboxylic acid

Prepared by proceeding in a similar manner to Intermediate 106, startingfrom tert-butyl (R)-1-ethylpyrrolidine-2-carboxylate (Intermediate 148)as a solid.

¹H NMR (CDCl₃) δ: 3.99 (1H, m), 3.76 (1H, dd), 3.37-3.23 (1H, m),3.21-3.08 (1H, m), 2.84 (1H, dt), 2.45-2.21 (2H, m), 2.07-1.94 (2H, m),1.39 (3H, t).

Intermediate 148: Benzyl (R)-1-ethylpyrrolidine-2-carboxylate

Prepared by proceeding in a similar manner to Intermediate 107, startingfrom benzyl (R)-pyrrolidine-2-carboxylate as a colourless oil.

¹H NMR (CDCl₃) δ: 7.34 (5H, m), 5.17 (2H, s), 3.19 (2H, m), 2.75 (1H,m), 2.45 (1H, m), 2.33 (1H, m), 2.12 (1H, m), 1.93 (2H, m), 1.81 (1H,m), 1.09 (3H, t).

Intermediate 149: (1-Ethylazetidin-3-yl)methylamine

A solution of 3-[bis-(tert-butoxycarbonylamino)methyl]-1-ethylazetidine(Intermediate 150, 0.83 g) in a mixture of methanol (6 mL) andconcentrated hydrochloric acid (1 mL) was stirred and heated at 50° C.for 3 hours. After cooling, the mixture was concentrated under vacuumand the residue was dissolved in isopropanol and treated with potassiumcarbonate (3 g). The mixture was stirred at room temperature for 48hours, then the solid was filtered off and the filtrate was evaporatedto dryness to give (1-ethylazetidin-3-yl)methylamine (0.18 g) as a lightsticky gum which was used without further characterisation.

Intermediate 150:3-[bis-(tert-Butoxycarbonylamino)methyl]-1-ethylazetidine

A mixture of acetaldehyde (1.5 g) and3-[bis-(tert-butoxycarbonyl-amino)methyl]azetidine (Intermediate 151,1.0 g) in ethanol (20 mL) was stirred at room temperature for 30 minutesand then 10% palladium on carbon (0.3 g) was added. The mixture wasstirred under an atmosphere of hydrogen overnight. The solid wasfiltered off and the filtrate was evaporated to dryness. The residue waspurified by chromatography on silica, eluting with a mixture of methanoland DCM (10%) to give3-[bis-(tert-butoxycarbonylamino)methyl]-1-ethylazetidine (0.83 g) as acolourless liquid, which was used without further characterization.

Intermediate 151: 3-[bis-(tert-Butoxycarbonylamino)methyl]azetidine

A mixture of3-[bis-(tert-butoxycarbonylamino)methyl]-1-(diphenylmethyl)azetidine(Intermediate 152, 6.4 g) and 10% palladium on carbon (3 g) in ethanol(100 mL) and acetic acid (2 mL) was stirred under an atmosphere ofhydrogen overnight. The solid was filtered off and the filtrate wasevaporated to dryness. The residue was dissolved in ethyl acetate andwashed with saturated aqueous sodium carbonate, dried (Na₂SO₄) andfiltered. The filtrate was evaporated to dryness and the residue waspurified by chromatography on silica, eluting with a mixture of methanoland DCM (10%) to give 3-[bis-(tert-butoxycarbonylamino)methyl]azetidine(4.0 g) as a colourless liquid, which was used without furthercharacterisation.

Intermediate 152:3-[bis-(tert-Butoxycarbonylamino)methyl]-1-(diphenylmethyl)-azetidine

Di-tert-butyl dicarbonate (22 g) was added to a solution of1-(diphenylmethyl)azetidin-3-ylmethylamine (5 g), DMAP (0.5 g) andtriethylamine (12 g) in THF (150 mL) and the resultant solution wasstirred and heated at 60° C. for 5 hours. After cooling, the mixture wasadded to brine solution and extracted with ethyl acetate, washed withbrine, dried (Na₂SO₄) and filtered. The filtrate was evaporated todryness and the residue was purified by chromatography on silica,eluting with a mixture of ethyl acetate and petroleum ether (10%) togive3-[bis-(tert-butoxycarbonylamino)methyl]-1-(diphenylmethyl)azetidine(6.4 g) as a white solid, which was used without furthercharacterisation.

Intermediate 153: Methyl(1aRS,7bSR)-5-[2-((Z)-3-diethylaminoprop-1-enyl)benzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

A mixture of methyl(1aRS,7bSR)-5-(2-bromobenzenesulfonylamino)-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate(Intermediate 154, 0.612 g),N,N-diethyl-N—((Z)-1-tributylstannanylprop-1-en-3-yl)amine (Intermediate11, 1.13 g), tri-tert-butylphosphonium tetrafluoroborate (0.041 g),tris-(dibenzylideneacetone)dipalladium (0.064 g) in dioxane (12 mL) andDMSO (0.4 mL) was degassed and purged with nitrogen then heated at 100°C. for 1.5 hours. After cooling, the mixture was diluted with brine andextracted with ethyl acetate. The organic layer was washed with water,dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness andthe residue was purified by chromatography on silica, eluting with amixture of methanol and DCM with a gradient of 0-15% to give methyl(1aRS,7bSR)-5-[2-((Z)-3-diethylamino-prop-1-enyl)benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.495 g) as a solid.

¹H NMR (CDCl₃) δ: 8.06 (1H, dd), 7.52 (1H, m), 7.40 (1H, m), 7.30 (1H,m), 7.14 (1H, d), 7.01 (1H, m), 6.86 (1H, d), 6.02 (1H, m), 4.33 (1H,d), 3.84 (3H, s), 3.77 (1H, d), 3.12 (2H, br s), 2.51 (4H, br s), 1.87(1H, m), 1.70 (1H, m), 1.05-0.85 (8H, m).

Intermediate 154: Methyl(1aRS,7bSR)-5-(2-bromobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

2-Bromobenzenesulfonyl chloride (0.559 g) was added to a solution ofmethyl(1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 42, 0.40 g) in DCM (12 mL) and pyridine (4 mL) and theresultant mixture was stirred at room temperature for 1 hour. Themixture was evaporated to dryness and the residue was dissolved in DCMand washed with 2N HCl, dried (Na₂SO₄) and filtered. The filtrate wasevaporated to dryness and the residue was purified by chromatography onsilica, eluting with a mixture of ethyl acetate and cyclohexane with agradient of 0-35% to give methyl(1aRS,7bSR)-5-(2-bromo-benzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.612 g) as a solid.

¹H NMR (CDCl₃) δ: 9.85 (1H, s), 7.89 (1H, dd), 7.85 (1H, dd), 7.57-7.49(2H, m), 7.26 (1H, d), 6.64 (1H, d), 4.27 (1H, d), 3.72 (1H, d), 3.66(3H, s), 2.05-1.95 (1H, m), 1.86-1.76 (1H, m), 1.08-0.98 (1H, m),0.84-0.76 (1H, m).

Intermediate 155: Methyl(1aRS,7bSR)-5-(2-{N—[((R)-1-ethylpyrrolidine-2-yl)carbonyl]-N-methylaminomethyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

HATU (0.136 g) was added to a mixture of methyl(1aRS,7bSR)-5-(4-fluoro-2-methylaminomethylbenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 156, 0.150 g), (R)-1-ethylpyrrolidine-2-carboxylic acid(Intermediate 147, 0.061 g) and N,N-diisopropyl-N-ethylamine (0.124 mL)in DMF (5 mL) and the mixture was stirred for 3 days at roomtemperature. The volatiles were removed in vacuo and the residue wasextracted with ethyl acetate (50 mL). The organic layer was washed withwater (50 mL), brine, dried (Na₂SO₄) and filtered. The filtrate wasevaporated to dryness and the residue was purified by chromatography onsilica eluting with a mixture of methanol and DCM with a gradient of0-10% to give methyl(1aRS,7bSR)-5-(2-{N—[((R)-1-ethylpyrrolidine-2-yl)carbonyl]methylamino]-methyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.177 g) as a solid.

LCMS (Method F) r/t 2.33 (M+H) 546.

Intermediate 156: Methyl(1aRS,7bSR)-5-(4-fluoro-2-methylaminomethylbenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

A solution of potassium carbonate (0.345 g) in water (2 mL) was added toa solution of methyl(1aRS,7bSR)-5-(4-fluoro-2-[N-methyl-N-(2,2,2-trifluoroacetyl)-aminomethyl]-benzenesulfonyl-amino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 157, 0.257 g) in methanol (12 mL) and the mixture washeated at 45° C. for 3 hours. After cooling, the volatiles were removedin vacuo and the residue was treated with water (30 mL) and saturatedwith sodium chloride and extracted with ethyl acetate (50 mL). Theorganic layer was dried (Na₂SO₄) and filtered and the filtrate wasevaporated to dryness to give methyl(1aRS,7bSR)-5-(4-fluoro-2-methylaminomethylbenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.156 g) as a solid.

LCMS (Method B) r/t 2.14 (M+H) 421.

Intermediate 157: Methyl(1aRS,7bSR)-5-(4-fluoro-2-[N-methyl-N-(2,2,2-trifluoroacetyl)-aminomethyl]benzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

A mixture of4-fluoro-2-[N-methyl-N-(2,2,2-trifluoroacetyl)aminomethyl]benzenesulfonylchloride (Intermediate 158, 0.182 g) was added to a solution of methyl(1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 42, 0.100 g) in DCM (3 mL) and pyridine (1 mL) and theresultant mixture was stirred at room temperature for 1 hour. Themixture was evaporated to dryness and the residue was purified bychromatography on silica eluting with a mixture of ethyl acetate andcyclohexane with a gradient of 0-40% to give methyl(1aRS,7bSR)-5-(4-fluoro-2-[N-methyl-N-(2,2,2-trifluoroacetyl)aminomethyl]benzenesulfonyl-amino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.257 g) as a solid.

LCMS (Method F) r/t 3.77 (M+H) 517.

Intermediate 158:4-Fluoro-2-[N-methyl-N-(2,2,2-trifluoroacetyl)aminomethyl]benzenesulfonylchloride

A solution of 3-fluoro-N-methyl-N-(trifluoroacetyl)benzylamine(Intermediate 159, 0.497 g) in DCE (0.5 mL) was added to stirred, cooledchlorosulfonic acid (3 mL). The mixture was allowed to come up to roomtemperature and then heated at 70° C. for 3 hours. After cooling, themixture was added carefully to a mixture of ice and water, thenextracted with ethyl acetate, washed with water, dried (MgSO₄) andfiltered. The filtrate was evaporated to dryness and the residue waspurified by chromatography on silica, eluting with a mixture of ethylacetate and pentane with a gradient of 2.5-10% to give4-fluoro-2-[N-methyl-N-(2,2,2-trifluoroacetyl)aminomethyl]-benzenesulfonylchloride (0.21 g) as a clear oil.

¹H NMR (CDCl₃) δ: 8.20 (1H, m), 7.24 (1H, m), 7.01 (1H, d), 5.21 (2H,s), 3.24 (2H, s), 3.13 (1H, s).

Intermediate 159: 3-Fluoro-N-methyl-N-(trifluoroacetyl)benzylamine

A solution of 3-fluoro-N-(trifluoroacetyl)benzylamine (Intermediate 105,0.508 g) in THF (5 mL) was added to a stirred suspension of sodiumhydride (60% oil dispersion, 0.096 g) in THF (5 mL). The resultantmixture was stirred at room temperature for 30 minutes. Iodomethane(0.653 g) was added and the mixture was stirred at room temperatureovernight. The mixture was poured into water and extracted with ethylacetate, washed with water, dried (MgSO₄) and filtered. The filtrate wasevaporated to dryness to give3-fluoro-N-methyl-N-(trifluoroacetyl)benzylamine (0.497 g) as a whitesolid.

¹H NMR (CDCl₃) δ: 7.34 (1H, m), 7.10-6.90 (3H, m), 4.63 (2H, s), 3.07(2H, q), 2.94 (1H, s).

Intermediate 160: Methyl(1aRS,7bSR)-5-(2-[N—((S)-1-ethylpyrrolidine-2-yl)carbonyl-N-methylaminomethyl]-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 155, startingfrom methyl(1aRS,7bSR)-5-(4-fluoro-2-methylaminomethylbenzenesulfonylamino)-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate(intermediate 156) and (S)-1-ethylpyrrolidine-2-carboxylic acid(Intermediate 106) as a solid/

LCMS (Method B) r/t 2.47 (M+H) 546.

Intermediate 161: Methyl(1aRS,7bSR)-5-[2-(4-dimethylaminobutylamino)-4-fluoro-benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4carboxylate

A solution of methyl(1aRS,7bSR)-5-(2,4-difluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate(Intermediate 162, 0.675 g) and N,N-dimethylbutane-diamine (0.496 g) indioxane (20 mL) was stirred and heated at 80° C. for 17 hours then leftat room temperature for 3 days. The solution was diluted with ethylacetate, washed with potassium carbonate solution and water then dried(Na₂SO₄) and filtered. The filtrate was concentrated in vacuo and theresidue was purified by chromatography on silica, eluting with a mixtureof methanol and DCM with a gradient of 0-40% to give methyl(1aRS,7bSR)-5-[2-(4-dimethyl-aminobutylamino)-4-fluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4carboxylate(0.499 g) as a colourless gum.

¹H NMR (CDCl₃) δ: 7.51 (1H, dd), 7.26 (1H, d), 7.12 (1H, d), 6.29 (2H,m), 6.00 (1H, br, s), 4.31 (1H, d), 3.75 (1H, d), 3.50 (3H, s), 3.01(2H, m), 2.25 (6H, s), 2.11 (2H, t), 1.94 (1H, m), 1.73 (1H, m), 1.58(4H, m), 1.03 (2H, m).

Intermediate 162: Methyl(1aRS,7bSR)-5-(2,4-difluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

2,4-Difluorobenzenesulphonyl chloride (0.468 g) was added to a solutionof methyl(1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylater(Intermediate 42, 0.438 g) in pyridine (2 mL) and DCM (4 mL) and thesolution was left at room temperature for 2 hours. The mixture wasdiluted with DCM, washed with 2M hydrochloric acid, dried (Na₂SO₄) andfiltered. The filtrate was concentrated in vacuo and the residue waspurified by chromatography on silica, eluting with a mixture of ethylacetate and cyclohexane with a gradient of 0-30% to give methyl(1aRS,7bSR)-5-(2,4-difluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.761 g) as a light coloured gum.

¹H NMR (CDCl₃) δ: 8.90 (1H, br, s), 7.82 (1H, m), 7.22 (1H, d), 7.13(1H, d), 6.88 (2H, m), 4.32 (1H, d), 3.89 (3H, s), 3.79 (1H, d), 1.90(1H, m), 1.71 (1H, m), 1.01 (2H, m).

Intermediate 163: ((R)-1-Ethylpyrrolidin-3-ylmethyl)amine

Lithium aluminium hydride was added to a stirred solution of((R)-1-acetylpyrrolidin-3-ylmethyl)amine (Intermediate 164, 1.5 g) inTHF (50 mL) and the resulting mixture was stirred and heated at refluxfor 2 hours. After cooling, ethanol was slowly added and the mixture wasconcentrated under vacuum. The residue was diluted with DCM and thesolid was filtered off. The filtrate was evaporated to dryness to give((R)-1-ethylpyrrolidin-3-ylmethyl)amine (0.9 g) as a yellow solid.

LCMS (Method D) r/t 0.396 (M+H) 129.

Intermediate 164: ((R)-1-Acetylpyrrolidin-3-ylmethyl)amine

A mixture of benzylN—((S)-1-acetylpyrrolidin-3-ylmethyl)-N-benzylcarbamate (Intermediate165, 4.2 g) and palladium hydroxide on carbon (0.4 g) in methanol (42mL) was stirred under an atmosphere of hydrogen at 60° C. for 48 hours.The mixture was filtered and the filtrate was evaporated to dryness togive ((R)-1-acetylpyrrolidin-3-ylmethyl)amine (1.5 g) as a light yellowoil.

LCMS (Method D) r/t 0.49 (M+H) 143.

Intermediate 165: BenzylN—((S)-1-acetylpyrrolidin-3-ylmethyl)-N-benzylcarbamate

Acetyl chloride (2.86 g) was added to a stirred solution of benzylN—((S)-pyrrolidin-3-ylmethyl)-N-benzylcarbamate (Intermediate 166, 5.9g) and triethylamine (3.68 g) in DCM (80 mL) with ice cooling. Theresultant mixture was stirred at room temperature for 2 hours thenconcentrated under vacuum. The residue was treated with saturatedaqueous sodium bicarbonate and extracted with ethyl acetate, dried(Na₂SO₄) and filtered. The filtrate was evaporated to dryness and theresidue was purified by chromatography on silica, eluting with ethylacetate to give benzylN—((S)-1-acetylpyrrolidin-3-ylmethyl)-N-benzylcarbamate (4.2 g) as ayellow oil.

LCMS (Method D) r/t 1.65 (M+H) 367.

Intermediate 166: Benzyl N—((S)-pyrrolidin-3-ylmethyl)-N-benzylcarbamate

tert-Butyl(S)-3-[N-benzyl-N-(benzyloxycarbonyl)aminomethyl]pyrrolidine-1-carboxylate(Intermediate 167, 11 g) was added dropwise to a solution of acetylchloride (15 g) in methanol (50 mL) and the resultant mixture wasstirred at room temperature overnight. The mixture was concentratedunder vacuum and the residue was purified by HPLC (C18) to give benzylN—((S)-pyrrolidin-3-ylmethyl)-N-benzylcarbamate (8.0 g) as an off whitesolid which was used without further characterisation.

Intermediate 167: tert-Butyl(S)-3-[N-benzyl-N-(benzyloxycarbonyl)aminomethyl]-pyrrolidine-1-carboxylate

A solution of tert-butyl(R)-3-(N-benzyloxycarbonyl)aminomethylpyrrolidine-1-carboxylate(Intermediate 168, 19 g) in DMF (90 mL) was added dropwise to asuspension of sodium hydride (60%, 4.55 g) in DMF (100 mL) Afterstirring for 30 minutes, benzyl bromide (11.7 g) was added dropwise. Theresultant mixture was stirred and heated at 70° C. overnight. Aftercooling, saturated aqueous sodium bicarbonate was added and the mixturewas extracted with ethyl acetate, dried (Na₂SO₄) and filtered. Thefiltrate was purified by chromatography on silica, eluting with amixture of ethyl acetate and petroleum ether (10%) to give tert-butyl(S)-3-[N-benzyl-N-(benzyloxycarbonyl)aminomethyl]-pyrrolidine-1-carboxylate(11.0 g) as a light yellow oil, which was used without furthercharacterisation.

Intermediate 168: tert-Butyl(R)-3-(N-benzyloxycarbonyl)aminomethylpyrrolidine-1-carboxylate

Benzyl chloroformate (14.1 g) was added dropwise to a cooled solution oftert-butyl (R)-3-aminomethylpyrrolidine-1-carboxylate (15 g) in THF (150mL) while maintaining the temperature below 0° C. On completion of theaddition, triethylamine (15.2 g) was added dropwise. The resultantmixture was stirred at −5° C. for 30 minutes then at room temperatureovernight. Brine was added and the mixture was extracted with ethylacetate, washed with brine, dried (Na₂SO₄) and filtered. The filtratewas evaporated to dryness to give tert-butyl(R)-3-(N-benzyloxycarbonyl)aminomethylpyrrolidine-1-carboxylate (23 g)as a colourless sticky gum, which was used without furthercharacterisation.

Intermediate 169: ((S)-1-Ethylpyrrolidin-3-yl)methylamine

Palladium on carbon (10%, 0.3 g) was added to a solution of benzylN—((S)-1-ethylpyrrolidin-3-ylmethyl)carbamate (Intermediate 170, 1.8 g)in methanol (20 mL) and the resultant mixture was stirred under anatmosphere of hydrogen for 24 hours. The mixture was filtered and thefiltrate was evaporated to dryness to give((S)-1-ethylpyrrolidin-3-yl)methylamine (0.8 g) as a colourless oil,which was used without further characterisation.

Intermediate 170: Benzyl N—((S)-1-ethylpyrrolidin-3-ylmethyl)carbamate

Iodoethane (4.1 g) was added to a cooled mixture of benzylN—((R)-pyrrolidin-3-ylmethyl)carbamate trifluoroacetate salt(Intermediate 171, 7.6 g) and potassium carbonate (12.2 g) in DMF (10mL) while maintaining the temperature at 0° C. The mixture was thenstirred at room temperature for 4 hours. Water was added and the mixturewas extracted with ethyl acetate, washed with brine, dried (Na₂SO₄) andfiltered. The filtrate was evaporated to dryness to give benzylN—((S)-1-ethylpyrrolidin-3-ylmethyl)carbamate (1.8 g) as a colourlessoil, which was used without further characterisation.

Intermediate 171: Benzyl N—((R)-pyrrolidin-3-ylmethyl)carbamatetrifluoroacetate salt

A mixture of tert-butyl(S)-3-(N-benzyloxycarbonyl)aminomethylpyrrolidine-1-carboxylate(Intermediate 172, 8.0 g) in trifluoroacetic acid (10 mL) was stirred atroom temperature for 5 hours. The mixture was concentrated under vacuumto give crude benzyl N—((R)-pyrrolidin-3-ylmethyl)carbamatetrifluoroacetate salt (7.6 g) as a light brown oil which was usedwithout further purification or characterisation.

Intermediate 172: tert-Butyl(S)-3-(N-benzyloxycarbonyl)aminomethylpyrrolidine-1-carboxylate

Prepared by proceeding in a similar manner to Intermediate 168, startingform tert-butyl (S)-3-aminomethylpyrrolidine-1-carboxylate and usedwithout further characterisation.

Intermediate 173: Methyl(1aRS,7bSR)-5-[2-(4-Ethyl-2-oxopiperazin-1-ylmethyl)-4-fluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

A solution of2-(4-ethyl-2-oxopiperazin-1-ylmethyl)-4-fluorobenzenesulfonyl chloride(Intermediate 174, 0.368 g) and methyl(1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate(Intermediate 42, 0.219 g) in pyridine (3 mL) and DCM (3 mL) was left tostand at room temperature for 17 hours. The mixture was evaporated invacuo and the residue was dissolved in water and DCM and the organiclayer was dried (Na₂SO₄) and filtered. The filtrate was concentrated invacuo and the residue was purified by chromatography on silica, elutingwith a mixture of ethyl acetate and cyclohexane with a gradient of50-100% to give a gum which was triturated with ether and filtered togive methyl(1aRS,7bSR)-5-[2-(4-ethyl-2-oxopiperazin-1-ylmethyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate(0.312 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 9.95 (1H, br, s), 7.81 (1H, dd), 7.26 (2H, m), 6.89(1H, dd), 6.59 (1H, d), 4.75 (2H, s), 4.29 (1H, d), 3.71 (1H, d), 3.62(3H, s), 3.15 (4H, m), 2.70 (2H, t), 2.45 (2H, q), 2.02 (1H, m), 1.72(1H, m), 1.06 (1H, m), 1.02 (3H, t), 0.80 (1H, q).

Intermediate 174:2-(4-Ethyl-2-oxopiperazin-1-ylmethyl)-4-fluorobenzenesulfonyl chloride

Chlorosulphonic acid (2 mL) was added to4-ethyl-1-(3-fluorobenzyl)-piperazin-2-one (Intermediate 175, 0.59 g)with stirring and cooling in ice. The cooling was removed and thesolution was stirred at room temperature for 4 hours before beingcarefully added to a mixture of ethyl acetate, ice and sodiumbicarbonate. The organic layer was dried (Na₂SO₄) and filtered and thefiltrate was concentrated in vacuo to give2-(4-ethyl-2-oxopiperazin-1-ylmethyl)-4-fluoro-benzenesulfonyl chloride(0.37 g) as a colourless gum.

LCMS (Method E) r/t 1.99 (M−H) 335, 337

Intermediate 175: 4-Ethyl-1-(3-fluoro-benzyl)-piperazin-2-one

Sodium hydride (60% oil dispersion, 0.176 g) was added to a stirredsolution of 4-ethyl-piperazin-2-one (Intermediate 176, 0.512 g) inanhydrous THF (10 mL) and the mixture was stirred at room temperaturefor 10 minutes. 3-Fluorobenzyl bromide (0.827 g) was added and stirringwas continued for 2 hours. The solution was diluted with water and ethylacetate and the organic layer was dried (Na₂SO₄) and filtered. Thefiltrate was concentrated in vacuo and the residue was purified bychromatography on silica, eluting with a mixture of methanol and DCMwith a gradient of 0-5% to give4-ethyl-1-(3-fluorobenzyl)piperazin-2-one (0.595 g) as a colourless oil.

¹H NMR (CDCl₃) δ: 7.26 (1H, m), 6.91-7.10 (3H, m), 4.61 (2H, s), 3.27(2H, t), 3.23 (2H, s), 2.65 (2H, t), 2.48 (2H, q), 1.09 (3H, t).

Intermediate 176: 4-Ethylpiperazin-2-one

A mixture of 2-oxopiperazine (1.07 g), iodoethane (1.72 g) and potassiumcarbonate (2.76 g) in acetonitrile (50 mL) was stirred at 55° C. for 3hours. After cooling, the mixture was filtered and the filtrate wasconcentrated in vacuo. The residue was triturated with DCM and filteredand the filtrate was concentrated in vacuo. The residue was purified bychromatography on silica, eluting with a mixture of methanol and DCMwith a gradient of 0-40% to give 4-ethylpiperazin-2-one (0.991 g) as acolourless oil.

¹H NMR (CDCl₃) δ: 6.81 (1H, br, s), 3.37 (2H, m), 3.14 (2H, s), 2.66(2H, t), 2.50 (2H, q), 1.11 (3H, t).

Intermediate 177: Methyl(1aRS,7bSR)-5-[2-(1-ethylpiperidin-4-ylmethyl)-4-fluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

2-(1-Ethylpiperidine-4-ylmethyl)-4-fluorobenzenesulfonyl chloride(Intermediate 178, 0.165 g) was added to a solution of methyl(1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(Intermediate 42, 0.290 g) in DCM (5 mL) and pyridine (1 mL) and theresultant mixture was stirred at room temperature for 21 hours. Themixture was evaporated to dryness and the residue was purified bychromatography on silica eluting with a mixture of 2M NH₃ in methanoland DCM with a gradient of 0-20% to give methyl(1aRS,7bSR)-5-[2-(1-ethyl-piperidin-4-ylmethyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(0.200 g) as a solid.

LCMS (Method F) r/t 2.34 (M+H) 503 Intermediate 178:2-(1-Ethylpiperidin-4-ylmethyl)-4-fluorobenzenesulfonyl chloride

A solution of 1-ethyl-4-(3-fluorobenzyl)piperidine (Intermediate 179,0.210 g) in DCE (1 mL) was added to chlorosulfonic acid (2 mL) at 0° C.The mixture was allowed to warm to room temperature and stirred for 2hours. The resultant mixture was added carefully to ice/water andextracted with DCM. The organic layer was dried (Na₂SO₄) and filteredand the filtrate was evaporated to dryness to give2-(1-ethylpiperidin-4-ylmethyl)-4-fluorobenzenesulfonyl chloride (0.290g) as a solid.

¹H NMR (CDCl₃) δ: 8.17 (1H, dd), 7.17 (1H, m), 7.08 (1H, dd), 3.59 (2H,d), 3.13-2.99 (4H, m), 2.57 (2H, m), 2.24 (2H, m), 1.95-1.77 (3H, m),1.47 (3H, t).

Intermediate 179: 1-Ethyl-4-(3-fluorobenzyl)piperidine

Bromoethane (0.1 mL) was added to a mixture of4-(3-fluorobenzyl)piperidine (Intermediate 180, 0.259 g) and potassiumcarbonate (0.204 g) in acetonitrile (10 mL). The mixture was stirred for20 hours then filtered. The filtrate acidified by addition of few dropsof 2M HCl and the solution was passed through a SCX-2 column (10 g). Theproduct was eluted with 2M ammonia in methanol and the residue afterevaporation was triturated with diethyl ether. The solid was filteredoff and the filtrated was concentrated in vacuo to give1-ethyl-4-(3-fluorobenzyl)piperidine (0.210 g)

¹H NMR (CDCl₃) δ: 7.24-7.16 (1H, m), 6.94-6.79 (3H, m), 2.91 (2H, dt),2.52 (2H, d), 2.36 (2H, q), 1.82 (2H, td), 1.68-1.57 (2H, m), 1.56-1.44(1H, m), 1.30 (2H, m), 1.06 (3H, t).

Intermediate 180: 4-(3-Fluorobenzyl)piperidine

A mixture of benzyl 4-(3-fluorobenzylidene)piperidine-1-carboxylate(Intermediate 181, 1.05 g), 20% palladium hydroxide on carbon (0.227 g),IMS (30 mL) and acetic acid (10 mL) was degassed by nitrogen/vacuumpurging. The mixture was placed under an atmosphere of hydrogen withrapid stirring. After 2 hours the mixture was filtered and the filtratewas diluted with water (40 mL) and neutralized with Na₂CO₃. The solutionwas saturated with sodium chloride, extracted with ethyl acetate dried(MgSO₄) and filtered. The filtrate was concentrated in vacuo and theresidue was dissolved in a mixture of methanol and water (20 mL, 1:1)and passed down a SCX-2 column. The product was eluted with 2M ammoniato give 4-(3-fluorobenzyl)piperidine (0.532 g)

¹H NMR (CDCl₃) δ: 7.24-7.16 (1H, m), 6.95-6.77 (3H, m), 3.04 (2H, dt),2.56 (2H, dd), 2.51 (2H, d), 1.71-1.54 (3H, m), 1.42 (1H, s), 1.14 (2H,m)

Intermediate 181: Benzyl 4-(3-fluorobenzylidene)piperidine-1-carboxylate

Sodium hydride (0.245 g) was added portionwise to a solution of diethyl(3-fluorobenzyl)phosphonate (Intermediate 182, Ig) in THF (40 mL) at 0°C. The mixture was stirred for 30 minutes then benzyl4-oxopiperidine-1-carboxylate (0.947 g) was added at 0° C. The mixturewas allowed to warm to room temperature and stirred for 21.5 hours. Themixture was partitioned between water and ethyl acetate and the organiclayer was washed with brine, dried (Na₂SO₄) and filtered. The filtratewas evaporated to dryness and the residue was purified by chromatographyon silica eluting with a mixture of ethyl acetate and cyclohexane with agradient of 0-25% to give benzyl4-(3-fluorobenzylidene)piperidine-1-carboxylate (1.05 g) ¹H NMR (CDCl₃)δ: 7.39-7.22 (6H, m), 6.98-6.83 (3H, m), 6.33 (1H, s), 5.15 (2H, s),3.54 (4H, dt), 2.41 (4H, dt).

Intermediate 182: Diethyl (3-fluorobenzyl)phosphonate

A mixture of 3-fluorobenzyl bromide (2 g) and triethyl phosphite (2.2mL) was heated at 160° C. under nitrogen for 4 hours. After cooling, thewere volatiles removed in vacuo and the residue was purified bychromatography on silica eluting with a mixture of ethyl acetate andcyclohexane with a gradient of 0-100% to give diethyl(3-fluorobenzyl)phosphonate (2.46 g)

¹H NMR (CDCl₃) δ: 7.31-7.22 (1H, m), 7.11-6.89 (3H, m), 4.09-3.97 (4H,m), 3.13 (2H, d), 1.25 (6H, t).

Intermediate 183: Methyl(1aRS,7bSR)-5-{2-[2-(1-ethylazetidin-3-yl)ethyl]-4-fluorobenzene-sulfonylamino})-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

A solution of tert-butyl(1aRS,7bSR)-3-{2-[5-fluoro-2-(4-methoxycarbonyl-1,1a,2,7b-tetrahydrocyclopropa[c]chromen-5-ylsulfamoyl)phenyl]ethyl}azetidine-1-carboxylate(Intermediate 184, 0.397 g) in DCM (5 mL) and trifluoroacetic acid (5mL) was left at room temperature for 30 minutes then evaporated in vacuoand the residue was dissolved in toluene and re-evaporated. The residuewas dissolved in DCM (15 mL) and acetaldehyde (0.063 g) was addedfollowed by sodium triacetoxyborohydride (0.301 g). The mixture wasstirred at room temperature for 2 hours then diluted with ethyl acetateand water and the organic layer was dried (Na₂SO₄) and filtered. Thefiltrate was concentrated in vacuo and the residue was purified bychromatography on silica, eluting with a mixture of methanol and DCMwith a gradient of 0-25% to give methyl(1aRS,7bSR)-5-{2-[2-(1-ethylazetidin-3-yl)ethyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.312 g) as a white foam.

LCMS (Method E) r/t 2.75 (M+H) 489.

Intermediate 184: tert-butyl(1aRS,7bSR)-3-{2-[5-fluoro-2-(4-methoxycarbonyl-1,1a,2,7b-tetrahydro-cyclopropa[c]chromen-5-ylsulfamoyl)phenyl]ethyl}azetidine-1-carboxylate

A mixture of tert-butyl(1aRS,7bSR)-3-{(E/Z)-2-[5-fluoro-2-(4-methoxycarbonyl-1,1a,2,7b-tetrahydrocyclopropa[c]chromen-5-ylsulfamoyl)phenyl]vinyl}azetidine-1-carboxylate(Intermediate 185, 0.502 g) and 10% palladium on carbon (0.05 g) inethanol (25 mL) was stirred under an atmosphere of hydrogen for 30minutes. The suspension was filtered and the filtrate was concentratedin vacuo. The residue was purified by chromatography on silica, elutingwith a mixture of ethyl acetate and cyclohexane with a gradient of 0-40%to give tert-butyl(1aRS,7bSR)-3-{2-[5-fluoro-2-(4-methoxycarbonyl-1,1a,2,7b-tetrahydrocyclopropa[c]chromen-5-ylsulfamoyl)phenyl]-ethyl}azetidine-1-carboxylate(0.401 g) as a colourless gum.

¹H NMR (CDCl₃) δ: 9.01 (1H, br, s), 7.90 (1H, dd), 7.21 (1H, d), 7.02(1H, d), 6.94 (2H, m), 4.32 (1H, d), 4.00 (2H, t), 3.79 (1H, d), 3.77(3H, s), 3.56 (2H, dd), 2.79 (2H, dd), 2.56 (1H, m), 1.89 (3H, m), 1.72(1H, m), 1.45 (9H, s), 0.99 (2H, m).

Intermediate 185: tert-Butyl(1aRS,7bSR)-3-{(E/Z)-2-[5-fluoro-2-(4-methoxycarbonyl-1,1a,2,7b-tetrahydro-cyclopropa[c]chromen-5-ylsulfamoyl)phenyl]vinyl}azetidine-1-carboxylate

A mixture of methyl(1aRS,7bSR)-5-(2-bromo-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 41, 0.456 g), tert-butyl3-((E/Z)-2-trimethylstannanylvinyl)azetidine-1-carboxylate (Intermediate186, 0.433 g), tris(dibenzylideneacetone)dipalladium(0) (0.046 g) andtri-tert-butylphosphonium tetrafluoroborate (0.029 g) in dioxane (15 mL)and DMSO (1.5 mL) was stirred and heated at 90° C. under nitrogen for 1hour. After cooling, the solution was diluted with ethyl acetate, washedwith water, dried (Na₂SO₄) and filtered. The filtrate was concentratedin vacuo and the residue was purified by chromatography on silica,eluting with a mixture of ethyl acetate and cyclohexane with a gradientof 0-40% to give tert-butyl(1aRS,7bSR)-3-{(E/Z)-2-[5-fluoro-2-(4-methoxycarbonyl-1,1a,2,7b-tetrahydrocyclopropa[c]chromen-5-ylsulfamoyl)phenyl]vinyl}-azetidine-1-carboxylate(0.508 g) as a colourless gum.

LCMS (Method E) r/t 4.47 (M−H) 557 Intermediate 186: tert-Butyl3-((E/Z)-2-trimethylstannanylvinyl)azetidine-1-carboxylate

A solution of tert-butyl 3-((E/Z)-2-iodovinyl)azetidine-1-carboxylate(Intermediate 187, 1.39 g), hexamethylditin (2.95 g), andtetrakis(triphenylphosphine)palladium(0) (0.52 g) in anhydrous THF (40mL) was stirred and heated at 50° C. under nitrogen for 2 hours. Aftercooling, the mixture was evaporated in vacuo and the residue waspurified by chromatography on silica, eluting with a mixture of ethylacetate and cyclohexane with a gradient of 0-10% to give tert-butyl3-((E/Z)-2-trimethylstannanylvinyl)azetidine-1-carboxylate (0.601 g) asa pale yellow oil.

¹H NMR (CDCl₃) δ: 5.79-6.5 (2H, m), 3.95 (2H, m), 3.62 (2H, m),2.88-3.12 (1H, m), 1.32 (9H, s), 0.0 (9H, s).

Intermediate 187: tert-Butyl3-((E/Z)-2-iodovinyl)azetidine-1-carboxylate

A solution of tert-butyl 3-formylazetidine-1-carboxylate (1.97 g) andiodoform (8.37 g) in anhydrous THF (25 mL) was added to a stirredsuspension of anhydrous chromium(II) chloride in anhydrous THF (100 mL)under nitrogen and the mixture was stirred at room temperature for 4hours. The resulting mixture was diluted with water and ethyl acetateand the organic layer was dried (Na₂SO₄) and filtered. The filtrate wasconcentrated in vacuo and the residue was purified by chromatography onsilica, eluting with a mixture of ethyl acetate and cyclohexane with agradient of 0-15% to give tert-butyl3-((E/Z)-2-iodovinyl)azetidine-1-carboxylate (2.01 g) as a pale yellowoil.

¹H NMR (CDCl₃) δ: 6.71 (0.8H, dd), 6.55 (0.2H, t), 6.33 (0.2H, d), 6.18(0.8H, d), 4.20 (0.4H, t), 4.08 (1.6H, t), 3.76 (2H, m), 3.45 (0.2H, m),3.19 (0.8H, m), 1.44 (9H, s).

Intermediate 188: Methyl(1aRS,7bSR)-5-(2-{[((S)-1-ethylpyrrolidine-3-carbonyl)amino]-methyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

HATU (0.234 g) was added to a mixture of(S)-1-ethylpyrrolidine-3-carboxylic acid (Intermediate 189, 0.089 g) andNMM (0.068 mL) in DMF (4 mL) and the mixture was stirred for 15 minutes.Methyl(1aRS,7bSR)-5-(2-aminomethyl-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 102, 0.250 g) was added and the mixture was stirred for 20hours. The mixture was diluted with water and extracted with ethylacetate. The organic layer was washed with saturated NaHCO₃ solution,dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness andthe residue was purified by chromatography on silica eluting with amixture of 2M ammonia in methanol and DCM with a gradient of 0-15% togive methyl(1aRS,7bSR)-5-(2-{[((S)-1-ethylpyrrolidine-3-carbonyl)amino]methyl}-4-fluoro-benzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.190 g) as a solid.

¹H NMR (CDCl₃) δ: 7.81 (1H, dd), 7.46-7.38 (1H, m), 7.30-7.20 (3H, m),7.06-6.93 (2H, m), 4.58 (2H, d), 4.32 (1H, dd), 3.79 (1H, dd), 3.76 (3H,s), 2.93-2.78 (3H, m), 2.70-2.49 (4H, m), 2.24-2.08 (1H, m), 2.00-1.87(2H, m), 1.78-1.68 (1H, m), 1.15 (3H, t), 1.06-0.98 (2H, m)

Intermediate 189: (S)-1-Ethyl-pyrrolidine-3-carboxylic acid

A mixture of benzyl (S)-1-ethylpyrrolidine-3-carboxylate (Intermediate190, 0.563 g), 20% palladium hydroxide on carbon (0.056 g), ethylacetate (9 mL) and IMS (1 mL) was degassed and hydrogenated for 4 hours.The catalyst was removed by filtration, washed with ethyl acetate andthe filtrate was concentrated in vacuo to give(S)-1-ethylpyrrolidine-3-carboxylic acid (0.318 g) as a solid.

¹H NMR (CDCl₃) δ: 12.46-10.55 (1H, br s), 3.84-3.57 (1H, br s),3.49-3.26 (1H, br s), 3.26-2.93 (5H, m), 2.50-2.33 (1H, m), 2.28-2.11(1H, m), 1.35 (3H, t).

Intermediate 190: Benzyl (S)-1-ethylpyrrolidine-3-carboxylate

Ethyl bromide (0.21 mL) was added to a mixture of benzyl(S)-pyrrolidine-3-carboxylate trifluoroacetic acid salt (Intermediate191, 0.897 g), potassium carbonate (0.971 g) and DMF (10 mL) at roomtemperature and the mixture was stirred for 25 hours. Further ethylbromide (0.1 mL) was added and stirring was continued for 24 hours.Further ethyl bromide (0.05 mL) was added and stirring was continued for22 hours. The resultant mixture was diluted with water and extractedwith diethyl ether, washed with brine, dried (Na₂SO₄) and filtered. Thefiltrate was concentrated in vacuo to give benzyl(S)-1-ethylpyrrolidine-3-carboxylate (0.563 g).

¹H NMR (CDCl₃) δ: 7.38-7.30 (5H, m), 5.13 (2H, s), 3.09 (1H, m), 2.93(1H, t), 2.76-2.66 (1H, m), 2.63 (1H, dd), 2.56-2.41 (3H, m), 2.16-2.05(2H, m), 1.10 (3H, t).

Intermediate 191: Benzyl (S)-pyrrolidine-3-carboxylate trifluoroaceticacid salt

Trifluoroacetic acid (2.5 mL) was added to a solution of benzyl(S)-1-tert-butoxycarbonylpyrrolidine-3-carboxylate (Intermediate 192,0.859 g) and DCM (10 mL) at room temperature. The mixture was stirredfor 4 hours then concentrated in vacuo. The residue was azetroped withtoluene then ethyl acetate to give benzyl (S)-pyrrolidine-3-carboxylatetrifluoroacetic acid salt (Ig).

¹H NMR (CDCl₃) δ: 7.41-7.29 (5H, m), 5.16 (2H, dd), 3.64-3.45 (2H, m),3.44-3.23 (3H, m), 2.42-2.20 (2H, m).

Intermediate 192; Benzyl(S)-1-tert-butoxycarbonylpyrrolidine-3-carboxylate

DBU (0.764 mL) was added to a mixture of benzyl bromide (0.61 mL),(S)-1-tert-butoxycarbonyl-pyrrolidine-3-carboxylic acid (Ig) inanhydrous toluene (10 mL) and the mixture was stirred at roomtemperature for 24 hours. The mixture was filtered and the filtrate wasconcentrated in vacuo. The residue was purified by chromatography onsilica eluting with a mixture of ethyl acetate and cyclohexane with agradient of 0-35% to give benzyl(S)-1-tert-butoxycarbonylpyrrolidine-3-carboxylate (0.859 g)

¹H NMR (CDCl₃) δ: 7.39-7.29 (5H, m), 5.14 (2H, s), 3.70-3.41 (3H, m),3.41-3.27 (1H, m), 3.08 (1H, m), 2.13 (2H, q), 1.45 (9H, s).

Intermediate 193: (R)-1-Ethylpyrrolidin-3-ylamine

Acetyl chloride (15 mL) was added to methanol (120 mL) and the resultantsolution was stirred for 20 minutes. A solution of tert-butylN—((R)-1-ethylpyrrolidin-3-yl)carbamate (Intermediate 94, 8.4 g) inmethanol (30 mL) was then added and the mixture was stirred and heatedat 80° C. overnight. After cooling, the mixture was concentrated undervacuum and the residue was redissolved in methanol (150 mL) andpotassium carbonate (25.8 g) was added. The mixture was stirred andheated at 30° C. for 30 hours. After cooling, the solid was filtered offand the filtrate was distilled, collecting the product at 100° C. togive (R)-1-ethylpyrrolidin-3-ylamine (2.10 g) as a yellow oil, which wasused without further characterisation.

Intermediate 194: (S)-1-Ethylpyrrolidin-3-ylamine

Prepared by proceeding in a similar manner to Intermediate 193, startingfrom tert-butyl N—((S)-1-ethylpyrrolidin-3-yl)carbamate (Intermediate82) and used without further characterisation.

Intermediate 195: Methyl(1aRS,7bSR)-5-(2-{[((R)-1-ethylpyrrolidine-3-carbonyl)amino]-methyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 188, startingfrom methyl(1aRS,7bSR)-5-(2-aminomethyl-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate(intermediate 102) and (R)-1-ethylpyrrolidine-3-carboxylic acid(Intermediate 196).

¹H NMR (CDCl₃) δ: 7.81 (1H, dd), 7.43-7.34 (1H, m), 7.30-7.20 (3H, m),7.05-6.93 (2H, m), 4.59 (2H, d), 4.32 (1H, dd), 3.79 (1H, dd), 3.76 (3H,s), 2.99-2.84 (3H, m), 2.81-2.73 (1H, m), 2.73-2.60 (3H, m), 2.27-2.12(1H, m), 2.01-1.88 (2H, m), 1.78-1.67 (1H, m), 1.17 (3H, s), 1.08-0.98(2H, m).

Intermediate 196: (R)-1-Ethylpyrrolidine-3-carboxylic acid

Prepared by proceeding in a similar manner to Intermediate 189, startingfrom benzyl (R)-1-ethylpyrrolidine-3-carboxylate (Intermediate 197).

¹H NMR (CDCl₃) δ: 11.05-9.55 (1H, br s), 3.71 (1H, br s), 3.37 (1H, brs), 3.27-2.94 (5H, m), 2.49-2.32 (1H, m), 2.29-2.13 (1H, m), 1.35 (3H,t).

Intermediate 197: Benzyl (R)-1-ethylpyrrolidine-3-carboxylate

Prepared by proceeding in a similar manner to Intermediate 190, startingfrom benzyl (R)-pyrrolidine-3-carboxylate trifluoroacetic acid salt(Intermediate 198).

¹H NMR (CDCl₃) δ: 7.38-7.30 (5H, m), 5.13 (2H, s), 3.09 (1H, m), 2.93(1H, t), 2.76-2.66 (1H, m), 2.63 (1H, dd), 2.52-2.42 (3H, m), 2.16-2.06(2H, m), 1.11 (3H, t).

Intermediate 198: Benzyl (R)-pyrrolidine-3-carboxylic trifluoroaceticacid salt

Prepared by proceeding in a similar manner to Intermediate 191, startingfrom benzyl (R)-1-tert-butoxycarbonylpyrrolidine-3-carboxylate(Intermediate 199).

¹H NMR (CDCl₃) δ: 7.41-7.29 (5H, m), 5.16 (2H, dd), 3.64-3.45 (2H, m),3.42-3.23 (3H, m), 2.41-2.20 (2H, m).

Intermediate 199: Benzyl(R)-1-tert-butoxycarbonylpyrrolidine-3-carboxylate

Prepared by proceeding in a similar manner to Intermediate 192, startingfrom (R)-1-tert-butoxycarbonyl-pyrrolidine-3-carboxylic acid.

¹H NMR (CDCl₃) δ: 7.42-7.29 (5H, m), 5.15 (2H, s), 3.72-3.42 (3H, m),3.42-3.26 (1H, m), 3.08 (1H, m), 2.13 (2H, q), 1.45 (9H, s).

Intermediate 200: Methyl(1aRS,7bSR)-5-{N-[2-((Z)-3-diethylamino-2-methylprop-1-enyl)-4-fluorobenzenesulfonyl]-N-(methoxycarbonyl)amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

Methanesulphonic anhydride (0.159 g) was added to a solution of methyl(1aRS,7bSR)-5-{N-[4-fluoro-2-((Z)-3-hydroxy-2-methylprop-1-enyl)benzenesulfonyl]-N-(methoxycarbonyl)amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 201, 0.310 g) and N,N-diisopropyl-N-ethylamine (0.118 g)in DCM (10 mL) and the mixture was left at room temperature for 1 hour.Diethylamine (1 mL) was added and the solution was left for a further 16hours. The mixture was washed with water and filtered through a phaseseparator. The filtrate was concentrated in vacuo and the residue waspurified by chromatography on silica, eluting with a mixture of methanoland DCM with a gradient of 0-8% to give methyl(1aRS,7bSR)-5-{N-[2-((Z)-3-diethylamino-2-methylprop-1-enyl)-4-fluorobenzene-sulfonyl]-N-methoxy-carbonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.268 g) as a white foam.

LCMS (Method E) r/t 2.79 (M+H) 561.

Intermediate 201: Methyl(1aRS,7bSR)-5-{N-[4-fluoro-2-((Z)-3-hydroxy-2-methylprop-1-enyl)benzenesulfonyl]-N-(methoxycarbonyl)amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

Concentrated hydrochloric acid (1 mL) was added to a solution of methyl(1aRS,7bSR)-5-(N-{2-[(Z)-3-(tert-butyldimethylsilanyloxy)-2-methylprop-1-enyl]-4-fluorobenzenesulfonyl]-N-methoxycarbonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 202, 0.385 g) in methanol (20 mL) and the mixture was leftat room temperature for 45 minutes. The solution was concentrated invacuo and the residue was purified by chromatography on silica, elutingwith a mixture of ethyl acetate and cyclohexane with a gradient of 0-60%to give methyl(1aRS,7bSR)-5-{N-[4-fluoro-2-((Z)-3-hydroxy-2-methylprop-1-enyl)benzenesulfonyl]-N-methoxycarbonylamino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(0.314 g) as a white foam.

¹H NMR (CDCl₃) δ: 8.18 (1H, dd), 7.35 (1H, d), 7.11 (1H, dt), 6.94 (1H,d), 6.89 (1H, d), 6.74 (1H, s), 4.39 (1H, d), 3.82-4.17 (3H, m), 3.76(1.5H, s), 3.72 (1.5H, s), 3.64 (3H, s), 1.98 (4H, m), 1.82 (1H, q),1.14 (2H, m).

Intermediate 202: Methyl(1aRS,7bSR)-5-(N-{2-[(Z)-3-(tert-butyldimethylsilanyloxy)-2-methylprop-1-enyl]-4-fluorobenzenesulfonyl]-N-(methoxycarbonyl)amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

A mixture of methyl(1aRS,7bSR)-5-[N-(2-bromo-4-fluorobenzenesulfonyl)-N-(methoxy-carbonyl)amino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate(Intermediate 65, 0.257 g),tert-butyl-dimethyl-((Z)-2-methyl-3-tributylstannanylallyloxy)silane(0.475 g), tris(dibenzylideneacetone)dipalladium(0) (0.023 g) andtri-tert-butylphosphonium tetrafluoroborate (0.015 g) in dioxane (8 mL)and DMSO (0.8 mL) was stirred and heated at 90° C. under nitrogen for 1hour. Further tris(dibenzylideneacetone)dipalladium(0) (0.023 g) andtri-tert-butylphosphonium tetrafluoroborate (0.015 g) were added andheating was continued for a further 40 minutes. After cooling, themixture was diluted with ethyl acetate, washed with water, dried(Na₂SO₄) and filtered. The filtrate was concentrated in vacuo and theresidue was purified by chromatography on silica, eluting with a mixtureof ethyl acetate and cyclohexane with a gradient of 0-20% to give methyl(1aRS,7bSR)-5-(N-{2-[(Z)-3-(tert-butyldimethylsilanyloxy)-2-methylprop-1-enyl]-4-fluorobenzenesulfonyl]-N-methoxycarbonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.231 g) as a colourless gum.

LCMS (Method E) r/t 5.22 (M+Na) 642.

Intermediate 203: 2-((R)-1-Ethylpyrrolidin-3-yl)ethylamine

Lithium aluminium hydride (1.0 g) was added in portions to a stirred,cooled solution of 2-((S)-1-ethylpyrrolidin-3-yl)acetonitrile(Intermediate 204, 3.8 g) in THF (20 mL) at 0° C. On completion of theaddition, the mixture was stirred at room temperature for 4 hours. Waterwas added cautiously, followed by addition of 15% aqueous sodiumhydroxide solution and more water. The solid was filtered off and thefiltrate was evaporated to dryness. The residue was dissolved in DCM,dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness togive 2-((R)-1-ethylpyrrolidin-3-yl)ethylamine (2.0 g) as a colourlessoil, which was used without further characterisation.

Intermediate 204: 2-((S)-1-Ethylpyrrolidin-3-yl)acetonitrile

Iodoethane (10.1 g) was added to a mixture of2-((S)-pyrrolidin-3-yl)acetonitrile hydrochloride (Intermediate 205, 7.9g) and potassium carbonate (29.7 g) in DMF (20 mL) and the resultantmixture was stirred at room temperature for 5 hours. Water was added andthe mixture was extracted with ethyl acetate, washed with brine, dried(Na₂SO₄) and filtered. The filtrate was evaporated to dryness to give2-((S)-1-ethylpyrrolidin-3-yl)acetonitrile (3.8 g) as a yellow oil whichwas used without further characterisation.

Intermediate 205: 2-((S)-Pyrrolidin-3-yl)acetonitrile hydrochloride

A solution of tert-butyl (S)-3-cyanomethylpyrrolidine-1-carboxylate(Intermediate 206, 12.3 g) in methanol (150 mL) and concentratedhydrochloric acid (12 mL) was stirred and heated at 50° C. overnight.After cooling, the mixture was concentrated under vacuum to give crude2-((S)-pyrrolidin-3-yl)acetonitrile hydrochloride (9.0 g) as a whitesolid which was used without further characterisation.

Intermediate 206: tert-Butyl (S)-3-cyanomethylpyrrolidine-1-carboxylate

A mixture of tert-butyl((R)-3-(4-methylbenzenesulfonyloxymethyl)pyrrolidine-1-carboxylate(Intermediate 207, 22.3 g) and sodium cyanide (6.13 g) in DMSO (100 mL)was stirred and heated at 100° C. for 4 hours. After cooling, asaturated aqueous solution of iron (II) sulphate was added and themixture was stirred at room temperature for 8 hours. The resultantmixture was extracted with ethyl acetate, washed with brine, dried(Na₂SO₄) and filtered. The filtrate was evaporated to dryness and theresidue was purified by chromatography on silica, eluting with anmixture of ethyl acetate and petroleum ether (20%) to give tert-butyl(S)-3-cyanomethylpyrrolidine-1-carboxylate (12.3 g) as a white solidwhich was used without further characterisation.

Intermediate 207: tert-Butyl((R)-3-(4-methylbenzenesulfonyloxymethyl)-pyrrolidine-1-carboxylate

Prepared by proceeding in a similar manner to Intermediate 140, startingfrom tert-butyl (R)-3-hydroxymethylpyrrolidine-1-carboxylate and4-methylbenzenesulfonyl chloride and used without furthercharacterisation.

Intermediate 208: 2-((S)-1-Ethylpyrrolidin-3-yl)ethylamine

Prepared by proceeding in a similar manner to Intermediate 203, startingfrom 2-((R)-1-ethylpyrrolidin-3-yl)acetonitrile (Intermediate 209) andused without further characterisation.

Intermediate 209: 2-((R)-1-Ethylpyrrolidin-3-yl)acetonitrile

Iodoethane (6.46 g) was added in portions to a cooled mixture of2-((R)-pyrrolidin-3-yl)acetonitrile (Intermediate 210, 4.6 g) andpotassium carbonate (8.6 g) in acetonitrile (30 mL) at 0° C. The mixturewas stirred for 3 hours at 0° C. then concentrated under vacuum. Theresidue was partitioned between water and DCM. The organic layer waswashed with brine, dried (Na₂SO₄) and filtered. The filtrate wasevaporated to dryness to give 2-((R)-1-ethylpyrrolidin-3-yl)acetonitrile(2.1 g) as a colourless liquid which was used without furthercharacterisation.

Intermediate 210: 2-((R)-Pyrrolidin-3-yl)acetonitrile hydrochloride

Prepared by proceeding in a similar manner to Intermediate 205, startingfrom tert-butyl (R)-3-cyanomethylpyrrolidine-1-carboxylate (Intermediate211) and used without further characterisation.

Intermediate 211: tert-Butyl (R)-3-cyanomethylpyrrolidine-1-carboxylate

Prepared by proceeding in a similar manner to Intermediate 206, startingfrom tert-butyl((S)-3-(4-methylbenzenesulfonyloxymethyl)pyrrolidine-1-carboxylate(Intermediate 212) and used without further characterisation.

Intermediate 212: tert-Butyl((S)-3-(4-methylbenzenesulfonyloxymethyl)-pyrrolidine-1-carboxylate

Prepared by proceeding in a similar manner to Intermediate 140, startingfrom tert-butyl (S)-3-hydroxymethylpyrrolidine-1-carboxylate and4-methylbenzenesulfonyl chloride and used without furthercharacterisation.

Intermediate 213: Methyl(1aR,7bS)-5-[2-((S)-1-ethylpyrrolidin-3-yloxymethyl)-4-fluoro-benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

A solution of tert-butyl (S)-3-[(1aR,7bS)-5-fluoro-2-(4-methoxycarbonyl-1,1a,2,7b-tetrahydro-cyclopropa[c]chromen-5-ylsulfamoyl)benzyloxy]pyrrolidine-1-carboxylate(Intermediate 214, 0.284 g) in trifluoroacetic acid (4 mL) and DCM (4mL) was left at room temperature for 30 minutes. The mixture wasevaporated in vacuo and the residue was azeotroped with toluene. Theresidue was dissolved in DCM (4 mL) and acetaldehyde (0.044 g) was addedfollowed by sodium triacetoxyborohydride (0.212 g). The mixture wasstirred at room temperature for 1 hour. The resulting solution wasdiluted with DCM and 1M sodium hydroxide solution and the organic layerwas dried (Na₂SO₄) and filtered. The filtrate was evaporated in vacuoand the residue was purified by chromatography on silica, eluting with amixture of methanol and DCM with a gradient of 0-20% to give methyl(1aR,7bS)-5-[2-((S)-1-ethylpyrrolidin-3-yloxymethyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.221 g) as a white foam.

¹H NMR (CDCl₃) δ: 7.76 (1H, dd), 7.32 (1H, dd), 7.16 (1H, d), 6.94 (1H,dt), 6.87 (1H, d), 4.86 (1H, d), 4.68 (1H, d), 4.32 (1H, d), 4.19 (1H,m), 3.79 (1H, d), 3.73 (3H, s), 3.13 (1H, d), 2.92 (1H, q), 2.35-2.75(4H, m), 2.10 (2H, m), 1.92 (1H, m), 1.72 (1H, m), 1.14 (3H, t), 1.03(2H, m).

Intermediate 214: tert-Butyl(S)-3-[(1aR,7bS)-5-fluoro-2-(4-methoxycarbonyl-1,1a,2,7b-tetrahydrocyclopropa[c]chromen-5-ylsulfamoyl)benzyloxy]pyrrolidine-1-carboxylate

A solution of tert-butyl(S)-3-(2-chlorosulfonyl-5-fluorobenzyloxy)pyrrolidine-1-carboxylate(Intermediate 215, 0.295 g) in DCM (2 mL) was added to a solution ofmethyl (1aR,7bS)-5-amino-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 42A, 0.11 g) in DCM (2 mL) and the mixture was left atroom temperature for 5 days. The mixture was diluted with DCM, washedwith 1M hydrochloric acid and filtered through a phase separator. Thefiltrate was evaporated in vacuo and the residue was purified bychromatography on silica, eluting with a mixture of ethyl acetate andcyclohexane with a gradient of 0-30% to give tert-butyl(S)-3-[5-fluoro-2-((1aR,7bS)-4-methoxycarbonyl-1,1a,2,7b-tetrahydrocyclopropa-[c]chromen-5-ylsulfamoyl)benzyloxy]pyrrolidine-1-carboxylate(0.288 g) as a white foam.

¹H NMR (CDCl₃) δ: 8.86 (1H, br, s), 7.76 (1H, dd), 7.41 (1H, dd), 7.25(1H, d), 7.07 (1H, d), 6.95 (1H, dt), 4.69-4.91 (2H, br, q), 4.32 (1H,d), 4.19 (1H, m), 3.77 (1H, d), 3.71 (3H, s), 3.49 (4H, br, m),1.89-2.18 (3H, m), 1.73 (1H, m), 1.47 (9H, s), 1.00 (2H, m).

Intermediate 215: tert-Butyl(S)-3-(2-chlorosulfonyl-5-fluorobenzyloxy)pyrrolidine-1-carboxylate

n-Butyllithium (1.6M in hexanes, 3.3 mL) was added to a solution oftert-butyl (S)-3-(2-bromo-5-fluorobenzyloxy)pyrrolidine-1-carboxylate(Intermediate 216, 1.87 g), in anhydrous THF (20 mL) at −78° C. under anatmosphere of nitrogen and the mixture was stirred for 30 minutes.Sulphur dioxide was passed through the resulting solution for 30minutes, then the cooling bath was removed and the mixture was allowedto warm to room temperature and stirred for 15 minutes. The solution wasevaporated in vacuo and the residue was dissolve in DCM (20 mL) andN-chlorosuccinimide (0.668 g) was added. The mixture was stirred for 30minutes then diluted with ether and water. The organic layer was dried(MgSO₄) and filtered and the filtrate was evaporated in vacuo. Theresidue was purified by chromatography on silica, eluting with a mixtureof ethyl acetate and cyclohexane with a gradient of 0-25% to givetert-butyl(S)-3-(2-chlorosulfonyl-5-fluorobenzyloxy)pyrrolidine-1-carboxylate(1.01 g) as a colourless, viscous oil.

¹H NMR (CDCl₃) δ: 8.09 (1H, dd), 7.58 (1H, dd), 7.18 (1H, dt), 4.98 (2H,q), 4.28 (1H, m), 3.40-3.61 (4H, m), 1.92-2.20 (2H, m), 1.47 (9H, s).

Intermediate 216: tert-Butyl(S)-3-(2-bromo-5-fluorobenzyloxy)pyrrolidine-1-carboxylate

Sodium hydride (60% oil dispersion, 0.24 g) was added to a stirredsolution of tert-butyl (S)-3-hydroxypyrrolidine-1-carboxylate (0.935 g)in THF (15 mL) and the mixture was stirred for 5 minutes.2-Bromo-5-fluorobenzyl bromide (1.608 g) was added and stirring wascontinued for 20 hours. The resultant suspension was filtered and thefiltrate was evaporated to dryness. The residue was purified bychromatography on silica, eluting with a mixture of ethyl acetate andcyclohexane with a gradient of 0-15% to give tert-butyl(S)-3-(2-bromo-5-fluorobenzyloxy)-pyrrolidine-1-carboxylate (1.88 g) asa colourless oil.

¹H NMR (CDCl₃) δ: 7.46 (1H, dd), 7.22 (1H, dd), 6.88 (1H, dt), 4.52 (2H,s), 4.19 (1H, m), 3.40-3.65 (4H, br, m), 1.91-2.18 (2H, m), 1.49 (9H,s).

Intermediate 217: Methyl(1aR,7bS)-5-[2-((R)-1-ethylpyrrolidin-3-yloxymethyl)-4-fluoro-benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 213, startingfrom tert-butyl(R)-3-[(1aR,7bS)-5-fluoro-2-(4-methoxycarbonyl-1,1a,2,7b-tetrahydrocyclopropa[c]chromen-5-ylsulfamoyl)benzyloxy]-pyrrolidine-1-carboxylate(Intermediate 218).

¹H NMR (CDCl₃) δ: 7.76 (1H, dd), 7.32 (1H, dd), 7.17 (1H, d), 6.95 (1H,dt), 6.88 (1H, d), 4.85 (1H, d), 4.68 (1H, d), 4.32 (1H, d), 4.18 (1H,m), 3.81 (1H, d), 3.72 (3H, s), 3.11 (1H, d), 2.92 (1H, q), 2.25-2.75(4H, m), 2.09 (2H, m), 1.91 (1H, m), 1.72 (1H, m), 1.14 (3H, t), 1.03(2H, m).

Intermediate 218: tert-Butyl (R)-3-[(1aR,7bS)-5-fluoro-2-(4-methoxycarbonyl-1,1a,2,7b-tetrahydrocyclopropa[c]chromen-5-ylsulfamoyl)benzyloxy]pyrrolidine-1-carboxylate

Prepared by proceeding in a similar manner to Intermediate 214, startingfrom tert-butyl(R)-3-(2-chlorosulfonyl-5-fluorobenzyloxy)pyrrolidine-1-carboxylate(Intermediate 219) and methyl (1aR,7bS)-5-amino-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 42A).

¹H NMR (CDCl₃) δ: 8.86 (1H, br, s), 7.76 (1H, dd), 7.41 (1H, dd), 7.25(1H, d), 7.07 (1H, d), 6.95 (1H, dt), 4.78 (2H, br, s), 4.32 (1H, d),4.19 (1H, m), 3.77 (1H, d), 3.71 (3H, s), 3.49 (4H, br, m), 1.89-2.18(3H, m), 1.73 (1H, m), 1.47 (9H, s), 1.00 (2H, m).

Intermediate 219: tert-Butyl(R)-3-(2-chlorosulfonyl-5-fluorobenzyloxy)pyrrolidine-1-carboxylate

Prepared by proceeding in a similar manner to Intermediate 215, startingfrom tert-butyl(R)-3-(2-bromo-5-fluorobenzyloxy)pyrrolidine-1-carboxylate (Intermediate220).

1H NMR (CDCl₃) δ: 8.10 (1H, dd), 7.58 (1H, dd), 7.17 (1H, dt), 4.99 (2H,q), 4.28 (1H, m), 3.40-3.61 (4H, m), 1.92-2.20 (2H, m), 1.48 (9H, s).

Intermediate 220: tert-Butyl(R)-3-(2-bromo-5-fluorobenzyloxy)pyrrolidine-1-carboxylate

Prepared by proceeding in a similar manner to Intermediate 216, startingfrom tert-butyl(R)-3-hydroxy-pyrrolidine-1-carboxylate.

¹H NMR (CDCl₃) δ: 7.46 (1H, dd), 7.22 (1H, dd), 6.88 (1H, dt), 4.52 (2H,s), 4.19 (1H, m), 3.40-3.65 (4H, br, m), 1.91-2.18 (2H, m), 1.49 (9H,s).

Intermediate 221: Methyl(1aR,7bS)-5-[2-(1-ethylpiperidin-3-ylmethyl)-4-fluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

2-(1-Ethylpiperidin-3-ylmethyl)-4-fluorobenzenesulfonyl chloride(Intermediate 222, 0.21 g) was added to a solution of methyl(1aR,7bS)-5-amino-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 42A 0.290 g) in DCM (10 mL) and pyridine (2 mL) and theresultant mixture was stirred at room temperature for 4 hours. Themixture was evaporated to dryness and the residue was partitionedbetween DCM and water. The organic layer was dried (Na₂SO₄), filteredand the filtrate was concentrated in vacuo. The residue was purified bychromatography on silica eluting with a mixture of 2M ammonia inmethanol and DCM with a gradient of 0-15% to give methyl(1aR,7bS)-5-[2-(1-ethylpiperidin-3-ylmethyl)-4-fluoro-benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(0.071 g).

¹H NMR (CDCl₃) δ: 7.95-7.88 (1H, m), 7.21-7.15 (1H, m), 7.03-6.86 (3H,m), 4.31 (1H, d), 3.81-3.73 (4H, m), 2.89-2.63 (4H, m), 2.39-2.28 (2H,m), 2.09-2.08-1.95 (1H, m), 1.94-1.44 (8H, m), 1.06-0.94 (6H, m).

Intermediate 222:2-(1-Ethylpiperidin-3-ylmethyl)-4-fluoro-benzenesulfonyl chloride

A solution of 1-ethyl-3-(3-fluorobenzyl)piperidine (Intermediate 223,0.214 g) in DCE (1 mL) was added to chlorosulfonic acid (2 mL) at 0° C.The mixture was allowed to warm to room temperature and stirred for 2hours. The mixture was added dropwise to a mixture of ice and brine andextracted with DCM. The organic layer was dried (Na₂SO₄) and filteredand the filtrate was evaporated to dryness to give2-(1-ethylpiperidin-4-ylmethyl)-4-fluorobenzene-sulfonyl chloride (0.44g) as a solid.

¹H NMR (CDCl₃) δ: 8.17-8.11 (1H, m), 7.43-7.37 (1H, m), 7.19-7.12 (1H,m), 3.62-3.52 (1H, m), 3.42-3.32 (1H, m), 3.16 (2H, d), 3.11-2.92 (3H,m), 2.64-2.29 (3H, m), 1.91 (2H, d), 1.43 (3H, t), 1.39-1.23 (1H, m).

Intermediate 223: 1-Ethyl-3-(3-fluorobenzyl)-piperidine

A solution of lithium aluminium hydride (2M in THF, 2.8 mL) was addeddropwise to a solution of 1-[3-(3-fluorobenzyl)piperidin-1-yl]ethanone(Intermediate 224, 0.66 g) in anhydrous THF (20 mL) at 0° C. underargon. The mixture was stirred for 30 minutes then allowed to warm toroom temperature and stirred for 2 hours. The mixture was recooled to 0°C. and water was added. The mixture was extracted with ether, washedwith brine, dried (Na₂SO₄) and filtered. The filtrate was evaporated todryness to give 1-ethyl-3-(3-fluorobenzyl)piperidine (0.535 g).

¹H NMR (CDCl₃) δ: 7.25-7.17 (1H, m), 6.95-6.80 (3H, m), 2.92-2.73 (2H,m), 2.58-2.42 (2H, m), 2.42-2.26 (2H, m), 1.96-1.76 (2H, m), 1.74-1.48(4H, m), 1.04 (3H, t), 1.00-0.84 (1H, m).

Intermediate 224: 1-[3-(3-Fluorobenzyl)piperidin-1-yl]ethanone

A mixture of 1-{3-[1-(3-fluorophenyl)methylidene]piperidin-1-yl}ethanone(Intermediate 225, 0.7 g), palladium hydroxide (20% on carbon, 0.07 g)in ethyl acetate (20 mL) and IMS (1 mL) was degassed by nitrogen/vacuumpurging. The mixture was stirred under an atmosphere of hydrogen for21.5 hours. The mixture was filtered the filtrate was evaporated todryness to give 1-[3-(3-fluorobenzyl)piperidin-1-yl]ethanone (0.66 g).

¹H NMR (CDCl₃) δ: 7.31-7.17 (1H, m), 6.97-6.80 (3H, m), 4.52-4.43 (0.5H,m), 4.41-4.31 (0.5H, m), 3.76-3.65 (0.5H, m), 3.65-3.55 (0.5H, m),3.07-2.95 (0.5H, m), 2.82-2.62 (1.5H, m), 2.60-2.49 (1H, m), 2.45-2.33(1H, m), 2.08 (1.5H, s), 1.95 (1.5H, s), 1.83-1.63 (3H, m), 1.50-1.32(1H, m), 1.29-1.09 (1H, m).

Intermediate 225:1-{3-[1-(3-Fluorophenyl)methylidene]piperidin-1-yl}ethanone

Acetyl chloride (0.515 mL) was added to a mixture of3-[1-(3-fluorophenyl)methylidene]-piperidine hydrochloride (Intermediate226, 1.5 g) and N,N-di-isopropyl-N-ethylamine (2.52 mL) in anhydrous THF(50 mL) at 0° C. under nitrogen. The mixture was allowed to warm to roomtemperature and was stirred for 2 hours. The mixture was diluted withwater (100 mL) and extracted with ether, washed with brine, dried(Na₂SO₄) and filtered. The filtrate was evaporated to dryness and theresidue was purified by chromatography on silica eluting with a mixtureof ethyl acetate and cyclohexane with a gradient of 75-100% to give1-{3-[1-(3-fluorophenyl)-methylidene]piperidin-1-yl}ethanone (1.38 g).

¹H NMR (CDCl₃) δ: 7.37-7.21 (1H, m), 7.04-6.82 (3H, m), 6.48-6.26 (1H,4s), 4.39-4.00 (2H, m), 3.72-3.48 (2H, m), 2.61-2.41 (2H, m), 2.18-2.02(3H, 4s), 1.83-1.61 (2H, m).

Intermediate 226: 3-[1-(3-Fluorophenyl)methylidene]piperidinehydrochloride

A solution of HCl in dioxane (4M, 30 mL) was added to a solution oftert-butyl 3-[1-(3-fluorophenyl)methylidene]piperidine-1-carboxylate(Intermediate 227, 2.38 g) in ether (30 mL) and the mixture was stirredat room temperature for 5 hours. The mixture was concentrated in vacuoand the residue was treated with ether. The solid was collected byfiltration, washed with ether and dried under vacuum to give3-[1-(3-fluorophenyl)methylidene]piperidine hydrochloride (1.64 g).

¹H NMR (CDCl₃) 3:2 ratio of E and Z isomers δ: 9.34 (2H, br s),7.48-7.37 (1H, m), 7.22-7.00 (3H, m), 6.59 (1H, s), 3.78-3.68 (2H, m),3.13 (2H, m), 2.52 (1.2H, m), 2.43 (0.8H, m), 1.84 (1.2H, m), 1.76(0.8H, m).

Intermediate 227: tert-Butyl3-[1-(3-fluorophenyl)methylidene]piperidine-1-carboxylate

(3-Fluorobenzyltriphenylphosphonium bromide (Intermediate 228, 5.3 g)was added in portions to a solution of sodium tert-butoxide (1.06 g) inanhydrous THF (20 mL) at room temperature and the mixture was stirredfor 30 minutes. A solution of tert-butyl 3-oxopiperidine-1-carboxylate(2 g) in anhydrous THF (10 mL) was added dropwise at room temperatureand the mixture was stirred for 24 hours. The mixture was diluted withwater (100 mL) and extracted with ether (100 mL), washed with brine,dried (Na₂SO₄) and filtered. The filtrate was concentrated in vacuo andthe residue was purified by chromatography on silica eluting with amixture of ethyl acetate and cyclohexane with a gradient of 0-20% togive tert-butyl3-[1-(3-fluorophenyl)-methylidene]piperidine-1-carboxylate (1.42 g).

¹H NMR (CDCl₃) 3:2 ratio of E and Z isomers δ: 7.33-7.21 (1H, m),7.05-6.85 (3H, m), 6.37 (0.6H, s), 6.28 (0.4H, s), 4.16 (0.8H, s), 4.00(1.2H, s), 3.50 (2H, t), 2.50 (1.2H, m), 2.39 (0.8H, m), 1.72 (0.8H, m),1.62 (1.2H, m), 1.48 (5.4H, s), 1.34 (3.6H, br s).

Intermediate 228: (3-Fluorobenzyl)triphenylphosphonium bromide

A mixture of 3-fluorobenzyl bromide (5 g) and triphenyl phosphine (6.94g) in toluene (50 mL) was heated at reflux for 3 hours. After cooling,the solid was collected by filtration, washed with toluene and driedunder vacuum at 50° C. to give (3-fluorobenzyl)triphenylphosphoniumbromide (10.1 g).

¹H NMR (DMSO-d₆) δ: 7.96-7.87 (3H, m), 7.81-7.64 (12H, m), 7.35-7.26(1H, m), 7.20-7.11 (1H, m), 6.88-6.82 (1H, m), 6.78-6.70 (1H, m), 5.21(2H, d).

Intermediate 229: Methyl (1aR,7bS)-5-{2-[2-((R)-1-ethylpyrrolidin-2-yl)ethyl]-4-fluoro-benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

Prepared by proceeding in a similar manner to Intermediate 95, startingfrom 2-[2-((R)-1-ethyl-pyrrolidin-2-yl)-ethyl]-4-fluorobenzenesulfonylchloride (intermediate 230) and methyl (1aR,7bS)-5-amino-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate(Intermediate 42A).

LCMS (Method A) r/t 2.30 (M+H) 503.

Intermediate 230:2-[2-((R)-1-Ethylpyrrolidin-2-yl)ethyl]-4-fluorobenzenesulfonyl chloride

Prepared by proceeding in a similar manner to intermediate 96, startingfrom (R)-1-ethyl-2-[2-(3-fluorophenyl)ethyl]pyrrolidine (intermediate231).

¹H NMR (CDCl₃) δ: 8.11 (1H, dd), 7.42 (1H, dd), 7.14 (1H, t), 3.93 (1H,m), 3.46-3.21 (2H, m), 3.13 (1H, m), 2.91 (2H, m), 2.43 (2H, m), 2.32(2H, m), 2.11 (3H, m), 1.50 (3H, t).

Intermediate 231: (R)-1-Ethyl-2-[2-(3-fluorophenyl)ethyl]pyrrolidine

A solution of 1-{(R)-2-[2-(3-fluorophenyl)ethyl]pyrrolidin-1-yl}ethanone(Intermediate 232, 0.48 g) in THF (20 mL) was cooled to 0° C. andtreated with a solution of lithium aluminum hydride (2M in THF, 3.6 mL)under an atmosphere of nitrogen. The resultant mixture was allowed towarm to room temperature before heating to 60° C. overnight. The mixturewas cooled to 0° C. and treated with water (0.35 ml), 4N sodiumhydroxide solution (0.35 ml) and further water (0.9 ml). Sodiumbisulphate powder was added to the suspension and the slurry wasfiltered through Celite and the filtrate was evaporated to dryness togive (R)-1-ethyl-2-[2-(3-fluoro-phenyl)ethyl]pyrrolidine (0.41 g) as anoil.

¹H NMR (CDCl₃) δ: 7.22 (1H, m), 6.96 (1H, d), 6.87 (2H, m), 3.18 (1H,dd), 2.87 (1H, m), 2.69 (1H, m), 2.55 (1H, m), 2.20 (1H, dq), 2.12-1.91(4H, m), 1.75 (2H, m), 1.54 (2H, m), 1.10 (3H, t). HNMR 205205

Intermediate 232:1-{(R)-2-[2-(3-Fluorophenyl)ethyl]pyrrolidin-1-yl}ethanone

Acetyl chloride (0.29 ml) was added to a solution ofN,N-diisopropyl-N-ethylamine (0.71 ml) and(R)-2-[2-(3-fluorophenyl)ethyl]-pyrrolidine (Intermediate 233, 0.39 g)in DCM (30 ml) and the mixture was stirred for 1.5 hours. The mixturewas washed with 1M HCl, dried (MgSO₄) and filtered. The filtrate wasevaporated to dryness to give1-{(R)-2-[2-(3-fluorophenyl)ethyl]-pyrrolidin-1-yl}ethanone (0.48 g) asan oil.

¹H NMR (d₆-DMSO, 80° C.) δ: 7.28 (1H, q), 7.02 (2H, t), 6.92 (1H, t),3.93 (1H, br s), 3.41 (2H, m), 2.60 (2H, m), 2.05-1.54 (6H, m), 1.90(3H, t).

Intermediate 233: (R)-2-[2-(3-Fluorophenyl)ethyl]pyrrolidine

Trifluoroacetic acid (5 mL) was added to a solution of tert-butyl(R)-2-[2-(3-fluorophenyl)ethyl]-pyrrolidine-1-carboxylate (Intermediate234, 0.55 g) in DCM (5 mL) and the mixture was stirred at roomtemperature for 1.5 hours. The mixture was evaporated to dryness and theresidue was dissolved in a small amount of methanol and loaded onto a 20g SCX-2 SPE cartridge, washed with methanol then eluted with 2M ammoniain methanol to give (R)-2-[2-(3-fluorophenyl)-ethyl]pyrrolidine (0.39g).

¹H NMR (CDCl₃) δ: 7.23 (1H, q), 6.97 (1H, d), 6.88 (2H, m), 2.99 (2H,m), 2.85 (1H, m), 2.69 (2H, m), 1.91 (1H, m), 1.75 (3H, m), 1.61 (1H, brs), 1.28 (1H, m).

Intermediate 234: tert-Butyl(R)-2-[2-(3-fluorophenyl)ethyl]pyrrolidine-1-carboxylate

A solution of tert-butyl(S)-2-(3-fluorophenylethynyl)pyrrolidine-1-carboxylate (Intermediate235, 1.26 g) in IMS (70 mL) was carefully added to 20% palladium oncarbon (0.6 g) under a carbon dioxide atmosphere. The mixture wasdegassed under vacuum and placed under an atmosphere of hydrogen. Thiswas repeated three times then the mixture was stirred under anatmosphere of hydrogen for 18 hours. The mixture was filtered throughCelite and the filtrate was evaporated to dryness. The residue waspurified by chromatography on silica, eluting with a mixture of DCM andpentane with a gradient of 0-100% to give tert-butyl(R)-2-[2-(3-fluoro-phenyl)ethyl]pyrrolidine-1-carboxylate (0.55 g) as anoil.

¹H NMR (CDCl₃) δ: 7.21 (1H, br m), 6.99-6.81 (3H, br m), 3.80 (1H, brd), 3.37 (2H, br d), 2.61 (2H, br m), 1.97 (2H, br m), 1.83 (2H, m),1.65 (2H, br m), 1.45 (9H, s).

Intermediate 235: tert-Butyl(S)-2-(3-fluorophenylethynyl)pyrrolidine-1-carboxylate

A suspension of 3-fluorobromobenzene (0.62 ml),tris(dibenzylideneacetone) dipalladium(0) (0.276 g),tri-tert-butylphosphonium tetrafluoroborate (0.165 g) and tert-butyl(S)-2-tributyl-stannanylethynylpyrrolidine-1-carboxylate (Intermediate236, 2.94 g) in anhydrous toluene (40 ml) was degassed under nitrogenand stirred at room temperature for 1.5 hours. The mixture wasevaporated to dryness and the residue was purified by chromatography onsilica, eluting with a mixture of DCM and pentane with a gradient of0-100% to give tert-butyl(S)-2-(3-fluoro-phenylethynyl)pyrrolidine-1-carboxylate (1.26 g) as anoil.

¹H NMR (CDCl₃) δ: 7.25 (1H, m), 7.16 (1H, br d), 7.08 (1H, br d), 6.99(1H, br t), 4.69 (1H, br d), 3.51 (1H, br s), 3.37 (1H, br s), 2.11 (3H,br m), 1.94 (1H, br s), 1.49 (9H, s).

Intermediate 236:tert-Butyl(S)-2-tributylstannanylethynylpyrrolidine-1-carboxylate

n-Butyl lithium (2.5M solution in hexanes. 11 mL) was added dropwise toa cooled solution of tert-butyl (S)-2-ethynylpyrrolidine-1-carboxylate(prepared according A Paul et al, Tetrahedron, 2006, 62, 8919, 4.49 g)in dry THF (230 ml) under an atmosphere of nitrogen while maintainingthe temperature below −65° C. When the addition was completed, themixture was stirred at −78° C. for 15 minutes then allowed to warm to 0°C. and stirred for 2.5 hours. Tributyl tin chloride (7.7 mL) was addeddropwise over five minutes and the mixture was stirred at roomtemperature for 1.5 hours. The mixture was cooled to 0° C. and saturatedsodium bicarbonate was added while maintaining the temperature below 15°C. The layers were separated and the aqueous layer was extracted withethyl acetate, washed with saturated sodium bicarbonate, water, dried(MgSO₄) and filtered. The filtrate was evaporated to dryness and theresidue was purified by chromatography on silica, eluting with a mixtureof pentane and ethyl acetate with a gradient of 0-7.5% to givetert-butyl (S)-2-tributylstannanylethynylpyrrolidine-1-carboxylate (0.39g) as an oil.

¹H NMR (CDCl₃) δ: 4.41 (1H, br s), 3.45 (1H, br m), 3.28 (1H, br s),2.03 (3H, br m), 1.86 (1H, br s), 1.54 (6H, m), 1.48 (9H, s), 1.33 (6H,q), 0.95 (6H, t), 0.90 (9H, t).

Biological Example

Compounds are tested for their capacity to inhibit recombinant humanMetAP2 activity using the following assay.

Human recombinant MetAP2 expressed in Sf9 cells followed by affinitypurification and EDTA treatment to remove endogenous active site cationwas dialysed against MnCl₂ to produce the manganese enzyme used in theassay. The assay was carried out for 30 minutes at 25° C. in 50 mM HEPESbuffer containing 100 mM NaCl, pH 7.5 the presence of 0.75 mMMethionine-Alanine-Serine (MAS) substrate and 50 μg/ml amino acidoxidase using a dilution of purified MetAP2 giving >3-fold signal:noise. Cleavage of the substrate by MetAP2 and oxidation of freemethionine by amino acid oxidase was detected and quantified usingfluorescence generated by Amplex red(10-acetyl-3,7-dihydroxyphenoxazine) in combination with horseradishperoxidase which detects H₂O₂ released during the oxidation step. Thefluorescent signal was detected using a multiwell fluorimeter. Compoundswere diluted in DMSO prior to addition to assay buffer, the final DMSOconcentration in the assay being 1%.

The IC₅₀ is defined as the concentration at which a given compoundachieves 50% inhibition of control. IC₅₀ values are calculated using theXLfit software package (version 2.0.5).

Compounds of the invention demonstrated activity in the assay of thisExample as indicated in the following table, wherein A represents <0.05μM, B represents IC₅₀ between 0.05 μM and 0.5 μM, and C representsIC₅₀>0.5 μM.

Compound name ActivityCis-(3aRS,9bRS)-7-(Benzenesulfonylamino)-1,3a,4,9b- Btetrahydro-2H-furo[2,3-c]chromene-6-carboxylic acidCis-(3aRS,9bRS)-7-[2-(3-Diethylaminopropyl)-4- Bfluorobenzenesulfonyl-amino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylic acidCis-(3aRS,9bRS)-7-[2-(3-{Pyrrolidin-1-yl}propyl)-4- Afluorobenzene-sulfonylamino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylic acidCis-(3aRS,9bRS)-7-[2-((Z)-3-Diethylaminoprop-1-enyl)-4- Afluoro-benzenesulfonylamino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylic acid First eluting enantiomer ofcis-(3aRS,9bRS)-7-[2-((Z)-3- ADiethylaminoprop-1-enyl)-4-fluoro-benzenesulfonylamino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylic acid Secondeluting enantiomer of cis-(3aRS,9bRS)-7-[2-((Z)-3- BDiethylaminoprop-1-enyl)-4-fluoro-benzenesulfonylamino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylic acid7-[2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl- Aamino]-1,2-dihydrofuro[2,3-c]quinoline-6-carboxylic acid formate salt7-(Benzenesulfonylamino))-1,2-dihydrofuro[2,3-c]quinoline-6- Acarboxylic acid formate saltCis-(3aRS,9bRS)-7-[2-((Z)-3-Diethylaminoprop-1-enyl)-4- Afluorobenzenesulfonylamino]-1,2,3a,4,5,9b-hexahydrofuro[2,3-c]quinoline-6-carboxylic acid5-[2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl- Aamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aS,7bR) 5-[2-((Z)-3-Diethylaminoprop-1-enyl)-4- Bfluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid (1aR,7bS)5-[2-((Z)-3-Diethylaminoprop-1-enyl)-4- Afluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-[2-((Z)-3-Diethylaminoprop-1-enyl)-4- Afluorobenzenesulfonylamino]-7b-methyl-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-[2-((E)-3-Diethylaminoprop-1-enyl)-4- Bfluorobenzenesulfonylamino]-7b-methyl-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acidCis-(3aRS,9bRS)-7-[2-(4-dimethylamino-butylamino)- Bbenzenesulfonylamino]-1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-6-carboxylic acid (1aR,7bS)-5-[2-(3-Diethylaminopropyl)-4- Afluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-[2-((Z)-3-Diethylaminoprop-1-enyl)-4- Afluorobenzene-sulfonylamino]-1,1-difluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid First elutingenantiomer of (1aRS,7bSR)-5-[2-((Z)-3- Bdiethylaminoprop-1-enyl)-4-fluorobenzene-sulfonylamino]-1,1-difluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4- carboxylic acidSecond eluting enantiomer of (1aRS,7bSR)-5-[2-((Z)-3- Adiethylaminoprop-1-enyl)-4-fluorobenzene-sulfonylamino]-1,1-difluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4- carboxylic acid(1aRS,7bSR)-5-[2((Z)-3-Ethylaminoprop-1-enyl)-4-fluoro- Abenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid First eluting enantiomer of(1aRS,7bSR)-5-[2((Z)-3- Aethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid Secondeluting enantiomer of (1aRS,7bSR)-5-[2((Z)-3- Bethylaminoprop-1-enyl)-4-fluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2[(Z)-3-(Pyrrolidin-1-yl)prop-1-enyl]-4- Afluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylic acid First eluting enantiomer of(1aRS,7bSR)-5-{2[(Z)-3-(pyrrolidin- B1-yl)prop-1-enyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylic acid Second elutingenantiomer of (1aRS,7bSR)-5-{2[(Z)-3- B(pyrrolidin-1-yl)prop-1-enyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-[2-(3-Dimethylaminopropylamino)benzene- Asulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4- carboxylicacid First eluting enantiomer of (1aRS,7bSR)-5-[2-(3- Cdimethylaminopropylamino)benzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid Second elutingenantiomer of (1aRS,7bSR)-5-[2-(3- Adimethylaminopropylamino)benzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-[2-(4-Dimethylaminobutylamino)benzene- Asulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4- carboxylicacid First eluting enantiomer of (1aRS,7bSR)-5-[2-(4- Bdimethylaminobutylamino)benzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid Second elutingenantiomer of (1aRS,7bSR)-5-[2-(4- Adimethylaminobutylamino)benzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-[2-(5-Dimethylaminopentylamino)benzene- Asulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4- carboxylicacid (1aRS,7bSR)-5-{2[(Z)-3-(propan-2-yl)aminoprop-1-enyl]-4- Bfluorobenzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2[(Z)-3-((S)-3-hydroxypyrrolidin-1- By)aminoprop-1-enyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2[(Z)-3-((R)-3-Hydroxypyrrolidin-1- Byl)aminoprop-1-enyl]-4-fluorobenzene-sulfonylamino}-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-[2((Z)-4-Diethylaminobut-1-enyl)-4- Afluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid First elutingenantiomer of (1aRS,7bSR)-5-[2((Z)-4- Bdiethylaminobut-1-enyl)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid Secondeluting enantiomer of (1aRS,7bSR)-5-[2((Z)-4- Bdiethylaminobut-1-enyl)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2-[2-(4-Ethylpiperazin-1-yl)-ethyl]-4- Bfluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2[(Z)-3-(Azetidin-1-yl)prop-1-enyl]-4- Bfluorobenzene-sulfonylamino}-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2[(Z)-3-(3-Hydroxyazetidin-1-yl)prop-1-enyl]- A4-fluorobenzene-sulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2[(Z)-3-(Azetidin-1-yl)propyl]-4- Bfluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-[2((Z)-4-Diethylaminobutyl)-4- Bfluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2-[N-(4-Dimethylaminobutyl)-N-methylamino]- Cbenzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2-[((S)-1-Ethylpyrrolidin-3-ylcarbamoyl)- Bmethyl]-4-fluoro-benzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-[2-(1-Ethylazetidin-3-yl)-4-fluorobenzene- Bsulfonylamino]-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4- carboxylicacid (1aRS,7bSR)-5-{2-[((R)-1-Ethylpyrrolidin-3-ylcarbamoyl)- Bmethyl]-4-fluorobenzenesulfonyl-amino}-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2-[2-(Pyrrolidin-1-yl)-ethyl]-4-fluorobenzene- Bsulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4- carboxylicacid (1aRS,7bSR)-5-[2-((R)-1-Ethylpyrrolidin-3-ylmethyl)-4- Afluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylic acid First eluting enantiomer of(1aRS,7bSR)-5-[2-((R)-1-ethyl- Bpyrrolidin-3-ylmethyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylic acid Secondeluting enantiomer of (1aRS,7bSR)-5-[2-((R)-1- AEthylpyrrolidin-3-ylmethyl)-4-fluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2-[((S)-1-Ethylpyrrolidin-2-yl)cabonyl- Aaminomethyl]-4-fluorobenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-[2-(4-Dimethylaminobutyrylamino)-4- Bfluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-[2-((S)-1-Ethyl-pyrrolidin-3-ylmethyl)-4- Bfluorobenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-[2-(3-Dimethylaminopropylcarbamoyl)benzene- Bsulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4- carboxylicacid (1aRS,7bSR)-5-(2-{[N-((S)-1-Ethyl-pyrrolidin-3-yl)-N-methyl- Bcarbamoyl]methyl}-4-fluoro-benzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-(2-{[N-((R)-1-Ethylpyrrolidin-3-yl)-N-methyl- Bcarbamoyl]methyl}-4-fluoro-benzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2-[2-((S)-1-Ethylpyrrolidin-2-yl)ethylamino]- Abenzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2-[2-((R)-1-Ethylpyrrolidin-2-yl)ethylamino]- Abenzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-[2-(3-N,N,-Diethylaminopropylamino)benzene- Asulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4- carboxylicacid (1aRS,7bSR)-5-(2-{[((R)-1-Ethylpyrrolidine-2-yl)carbonyl- Bamino]methyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2-[(1-Ethylazetidin-3-ylmethyl)amino]benzene- Bsulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4- carboxylicacid First eluting enantiomer of (1aRS,7bSR)-5-[2-((Z)-3- Bdiethylaminoprop-1-enyl)benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid Second elutingenantiomer of (1aRS,7bSR)-5-[2-((Z)-3- Adiethylaminoprop-1-enyl)benzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-(2-{N-[((R)-1-Ethylpyrrolidine-2-yl)carbonyl]- BN-methylaminomethyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-(2-{N-[((S)-1-Ethylpyrrolidine-2-yl)carbonyl]-N- Bmethylamino-methyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-[2-(4-Dimethylaminobutylamino)-4-fluoro- Bbenzenesulfonyl-amino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2-[((R)-1-Ethylpyrrolidin-3-ylmethyl)amino]- Bbenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2-[((S)-1-Ethylpyrrolidin-3-ylmethyl)amino]- Bbenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-[2-(4-Ethyl-2-oxopiperazin-1-ylmethyl)-4- Bfluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-[2-(1-Ethylpiperidin-4-ylmethyl)-4-fluoro- Abenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2-[2-(1-Ethylazetidin-3-yl)ethyl]-4-fluoro- Bbenzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2-[((S)-1-Azabicyclo[2.2.2]oct-3- Byl)amino]benzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2-[((R)-1-Azabicyclo[2.2.2]oct-3- Ayl)amino]benzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-(2-{[((S)-1-ethylpyrrolidine-3- Bcarbonyl)amino]methyl}-4-fluoro-benzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2-[2-((R)-1-Ethylpyrrolidin-3-ylamino)ethyl]-4- Bfluoro-benzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2-[((R)-1-Ethylpyrrolidin-3-yl)amino]- Bbenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2-[((S)-1-Ethylpyrrolidin-3-yl)amino]- Bbenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-(2-{[((R)-1-Ethylpyrrolidine-3-carbonyl)amino]- Bmethyl}-4-fluoro-benzenesulfonylamino)-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-[2-((Z)-3-Diethylamino-2-methylprop-1-enyl)-4- Afluorobenzene-sulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2-[2-((R)-1-Ethylpyrrolidin-3-yl)ethylamino]- Bbenzenesulfonylamino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid(1aRS,7bSR)-5-{2-[2-((S)-1-Ethylpyrrolidin-3-yl)ethylamino]- Bbenzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid(1aR,7bS)-5-[2-((S)-1-Ethylpyrrolidin-3-yloxymethyl)-4-fluoro- Bbenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid(1aR,7bS)-5-[2-((R)-1-Ethylpyrrolidin-3-yloxymethyl)-4-fluoro- Bbenzenesulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid(1aR,7bS)-5-[2-(1-Ethylpiperidin-3-ylmethyl)-4-fluorobenzene- Bsulfonylamino]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4- carboxylicacid (1aR,7bS)-5-{2-[2-((R)-1-Ethylpyrrolidin-2-yl)ethyl]-4- Bfluorobenzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid

INCORPORATION BY REFERENCE

All publications and patents mentioned herein, including those itemslisted below, are hereby incorporated by reference in their entirety forall purposes as if each individual publication or patent wasspecifically and individually incorporated by reference. In case ofconflict, the present application, including any definitions herein,will control.

EQUIVALENTS

While specific embodiments of the subject invention have been discussed,the above specification is illustrative and not restrictive. Manyvariations of the invention will become apparent to those skilled in theart upon review of this specification. The full scope of the inventionshould be determined by reference to the claims, along with their fullscope of equivalents, and the specification, along with such variations.

Unless otherwise indicated, all numbers expressing quantities ofingredients, reaction conditions, and so forth used in the specificationand claims are to be understood as being modified in all instances bythe term “about.” Accordingly, unless indicated to the contrary, thenumerical parameters set forth in this specification and attached claimsare approximations that may vary depending upon the desired propertiessought to be obtained by the present invention.

What is claimed is:
 1. A tricyclic compound represented by:

or a pharmaceutically acceptable salt or stereoisomer thereof.
 2. Atricyclic compound represented by:

or a pharmaceutically acceptable salt thereof.